JoVE Core Organic Chemistry Chapter 3.12: 대체 사이클로헥산의 안정성

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챕터 0: 공유결합과 구조

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JoVE Core Organic Chemistry Chapter 1.1: 유기 화학이란 무엇입니까?
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JoVE Core Organic Chemistry Chapter 1.2: 원자의 전자 구조
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JoVE Core Organic Chemistry Chapter 1.3: 전자 구성
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JoVE Core Organic Chemistry Chapter 1.4: 화학 채권
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JoVE Core Organic Chemistry Chapter 1.5: 극지 공유 채권
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JoVE Core Organic Chemistry Chapter 1.6: 루이스 구조 및 공식 요금
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JoVE Core Organic Chemistry Chapter 1.7: VSEPR 이론
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JoVE Core Organic Chemistry Chapter 1.8: 분자 기하학 및 일극의 순간
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JoVE Core Organic Chemistry Chapter 1.9: 공명 및 하이브리드 구조
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JoVE Core Organic Chemistry Chapter 1.10: 발렌스 본드 이론과 혼성 궤도
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JoVE Core Organic Chemistry Chapter 1.11: MO 이론 및 공유 본딩
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JoVE Core Organic Chemistry Chapter 1.12: 분자 간 힘 및 물리적 특성
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JoVE Core Organic Chemistry Chapter 1.13: 가용성
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JoVE Core Organic Chemistry Chapter 1.14: 기능그룹 소개
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JoVE Core Organic Chemistry Chapter 1.15: 고급 기능 그룹의 개요

챕터 0: 열역학과 화학반응속도론

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JoVE Core Organic Chemistry Chapter 2.1: 화학 반응
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JoVE Core Organic Chemistry Chapter 2.2: 엔탈피와 반응의 열
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JoVE Core Organic Chemistry Chapter 2.3: 솔루션 형성의 에너지
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JoVE Core Organic Chemistry Chapter 2.4: 엔트로피와 솔비
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JoVE Core Organic Chemistry Chapter 2.5: 깁스 무료 에너지 및 열역학적 호의
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JoVE Core Organic Chemistry Chapter 2.6: 화학 및 용해도 평형
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JoVE Core Organic Chemistry Chapter 2.7: 속도 법 및 반응 순서
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JoVE Core Organic Chemistry Chapter 2.8: 반응 속도에 대한 온도 변화의 영향
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JoVE Core Organic Chemistry Chapter 2.9: 다단계 반응
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JoVE Core Organic Chemistry Chapter 2.10: 채권 해리 에너지 및 활성화 에너지
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JoVE Core Organic Chemistry Chapter 2.11: 에너지 다이어그램, 전환 상태 및 중간
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JoVE Core Organic Chemistry Chapter 2.12: 반응 결과 예측

챕터 0: 알케인과 사이클로알케인

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JoVE Core Organic Chemistry Chapter 3.1: 알카네의 구조
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JoVE Core Organic Chemistry Chapter 3.2: 알카네의 헌법 이소머스
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JoVE Core Organic Chemistry Chapter 3.3: 알카인의 명칭
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JoVE Core Organic Chemistry Chapter 3.4: 알케인의 물리적 특성
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JoVE Core Organic Chemistry Chapter 3.5: 뉴먼 프로젝션
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JoVE Core Organic Chemistry Chapter 3.6: 에탄과 프로판의 적합성
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JoVE Core Organic Chemistry Chapter 3.7: 부탄의 적합성
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JoVE Core Organic Chemistry Chapter 3.8: 사이클로알카네인
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JoVE Core Organic Chemistry Chapter 3.9: 사이클로알카네인의 적합성
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JoVE Core Organic Chemistry Chapter 3.10: 사이클로헥산의 적합성
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JoVE Core Organic Chemistry Chapter 3.11: 사이클로헥산의 의자 형태
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JoVE Core Organic Chemistry Chapter 3.12: 대체 사이클로헥산의 안정성
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JoVE Core Organic Chemistry Chapter 3.13: 디대체 사이클로헥산: 시스 트랜스 이소머리즘
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JoVE Core Organic Chemistry Chapter 3.14: 연소 에너지: 알카네와 사이클로알카인의 안정성 측정

챕터 0: 입체 이성질

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JoVE Core Organic Chemistry Chapter 4.1: 키랄리티
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JoVE Core Organic Chemistry Chapter 4.2: 이소머리즘
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JoVE Core Organic Chemistry Chapter 4.3: 스테레오소머스
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JoVE Core Organic Chemistry Chapter 4.4: 명명 엔안티오메르
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JoVE Core Organic Chemistry Chapter 4.5: 엔안티오머 및 광학 활동의 특성
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JoVE Core Organic Chemistry Chapter 4.6: 다중 키랄 센터를 가진 분자
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JoVE Core Organic Chemistry Chapter 4.7: 피셔 프로젝션
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JoVE Core Organic Chemistry Chapter 4.8: 인종 혼합물과 엔안티오머의 해상도
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JoVE Core Organic Chemistry Chapter 4.9: 순환 화합물의 스테레오소머리즘
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JoVE Core Organic Chemistry Chapter 4.10: 질소, 인 및 황의 키랄리티
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JoVE Core Organic Chemistry Chapter 4.11: 프로시노성
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JoVE Core Organic Chemistry Chapter 4.12: 자연의 키랄리티

챕터 0: 산과 염기

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JoVE Core Organic Chemistry Chapter 5.1: 브뢰른스테드–Lowry 산및 기지
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JoVE Core Organic Chemistry Chapter 5.2: 루이스 산 및 기지
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JoVE Core Organic Chemistry Chapter 5.3: 산및염기: Ka,pKa,상대강점
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JoVE Core Organic Chemistry Chapter 5.4: 산염-염기 반응의 평형 위치
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JoVE Core Organic Chemistry Chapter 5.5: 분자 구조 및 산도
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JoVE Core Organic Chemistry Chapter 5.6: 레벨링 효과 및 비수성 산염 베이스 솔루션
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JoVE Core Organic Chemistry Chapter 5.7: 솔바팅 효과

챕터 0: 친핵성 치환과 알킬 할라이드 반응 제거

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JoVE Core Organic Chemistry Chapter 6.1: 알킬 할리데스
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JoVE Core Organic Chemistry Chapter 6.2: 뉴클레오필성 대체 반응
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JoVE Core Organic Chemistry Chapter 6.3: 뉴클레오필
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JoVE Core Organic Chemistry Chapter 6.4: 전기 애호가
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JoVE Core Organic Chemistry Chapter 6.5: 그룹 탈퇴
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JoVE Core Organic Chemistry Chapter 6.6: 카보케이션
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JoVE Core Organic Chemistry Chapter 6.7: SN2 반응: 운동학
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JoVE Core Organic Chemistry Chapter 6.8: SN2 반응: 메커니즘
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JoVE Core Organic Chemistry Chapter 6.9: SN2 반응: 전환 상태
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JoVE Core Organic Chemistry Chapter 6.10: SN2 반응: 스테레오케미스케
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JoVE Core Organic Chemistry Chapter 6.11: SN1 반응: 운동학
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JoVE Core Organic Chemistry Chapter 6.12: SN1 반응: 메커니즘
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JoVE Core Organic Chemistry Chapter 6.13: SN1 반응: 스테레오케미스케
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JoVE Core Organic Chemistry Chapter 6.14: 제품 예측: SN1 vs. SN2
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JoVE Core Organic Chemistry Chapter 6.15: 제거 반응
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JoVE Core Organic Chemistry Chapter 6.16: E2 반응: 운동 및 메커니즘
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JoVE Core Organic Chemistry Chapter 6.17: E2 반응: 스테레오케미케와 재조화학
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JoVE Core Organic Chemistry Chapter 6.18: E1 반응: 운동 및 메커니즘
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JoVE Core Organic Chemistry Chapter 6.19: E1 반응: 스테레오케미케와 재조화학
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JoVE Core Organic Chemistry Chapter 6.20: 제품 예측: 대체 대 제거

챕터 0: Alkene Structure and Reactivity

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JoVE Core Organic Chemistry Chapter 7.1: Structure and Bonding of Alkenes
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JoVE Core Organic Chemistry Chapter 7.2: Nomenclature of Alkenes
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JoVE Core Organic Chemistry Chapter 7.3: Degree of Unsaturation
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JoVE Core Organic Chemistry Chapter 7.4: Isomerism in Alkenes
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JoVE Core Organic Chemistry Chapter 7.5: Relative Stabilities of Alkenes
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JoVE Core Organic Chemistry Chapter 7.6: Introduction to Electrophilic Addition Reactions of Alkenes
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JoVE Core Organic Chemistry Chapter 7.7: Regioselectivity of Electrophilic Additions to Alkenes: Markovnikov's Rule

챕터 0: Reactions of Alkenes

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JoVE Core Organic Chemistry Chapter 8.1: Regioselectivity of Electrophilic Additions-Peroxide Effect
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JoVE Core Organic Chemistry Chapter 8.2: Free-Radical Chain Reaction and Polymerization of Alkenes
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JoVE Core Organic Chemistry Chapter 8.3: Halogenation of Alkenes
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JoVE Core Organic Chemistry Chapter 8.4: Formation of Halohydrin from Alkenes
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JoVE Core Organic Chemistry Chapter 8.5: Acid-Catalyzed Hydration of Alkenes
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JoVE Core Organic Chemistry Chapter 8.6: Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
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JoVE Core Organic Chemistry Chapter 8.7: Oxymercuration-Reduction of Alkenes
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JoVE Core Organic Chemistry Chapter 8.8: Hydroboration-Oxidation of Alkenes
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JoVE Core Organic Chemistry Chapter 8.9: Regioselectivity and Stereochemistry of Hydroboration
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JoVE Core Organic Chemistry Chapter 8.10: Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
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JoVE Core Organic Chemistry Chapter 8.11: Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate
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JoVE Core Organic Chemistry Chapter 8.12: Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
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JoVE Core Organic Chemistry Chapter 8.13: Oxidative Cleavage of Alkenes: Ozonolysis
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JoVE Core Organic Chemistry Chapter 8.14: Reduction of Alkenes: Catalytic Hydrogenation
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JoVE Core Organic Chemistry Chapter 8.15: Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

챕터 0: Alkynes

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JoVE Core Organic Chemistry Chapter 9.1: Structure and Physical Properties of Alkynes
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JoVE Core Organic Chemistry Chapter 9.2: Nomenclature of Alkynes
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JoVE Core Organic Chemistry Chapter 9.3: Acidity of 1-Alkynes
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JoVE Core Organic Chemistry Chapter 9.4: Preparation of Alkynes: Alkylation Reaction
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JoVE Core Organic Chemistry Chapter 9.5: Preparation of Alkynes: Dehydrohalogenation
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JoVE Core Organic Chemistry Chapter 9.6: Electrophilic Addition to Alkynes: Halogenation
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JoVE Core Organic Chemistry Chapter 9.7: Electrophilic Addition to Alkynes: Hydrohalogenation
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JoVE Core Organic Chemistry Chapter 9.8: Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration
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JoVE Core Organic Chemistry Chapter 9.9: Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
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JoVE Core Organic Chemistry Chapter 9.10: Alkynes to Carboxylic Acids: Oxidative Cleavage
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JoVE Core Organic Chemistry Chapter 9.11: Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
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JoVE Core Organic Chemistry Chapter 9.12: Reduction of Alkynes to trans-Alkenes: Sodium in Liquid Ammonia

챕터 0: Alcohols and Phenols

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JoVE Core Organic Chemistry Chapter 10.1: Structure and Nomenclature of Alcohols and Phenols
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JoVE Core Organic Chemistry Chapter 10.2: Physical Properties of Alcohols and Phenols
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JoVE Core Organic Chemistry Chapter 10.3: Acidity and Basicity of Alcohols and Phenols
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JoVE Core Organic Chemistry Chapter 10.4: Preparation of Alcohols via Addition Reactions
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JoVE Core Organic Chemistry Chapter 10.5: Preparation of Alcohols via Substitution Reactions
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JoVE Core Organic Chemistry Chapter 10.6: Acid-Catalyzed Dehydration of Alcohols to Alkenes
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JoVE Core Organic Chemistry Chapter 10.7: Alcohols from Carbonyl Compounds: Reduction
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JoVE Core Organic Chemistry Chapter 10.8: Alcohols from Carbonyl Compounds: Grignard Reaction
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JoVE Core Organic Chemistry Chapter 10.9: Protection of Alcohols
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JoVE Core Organic Chemistry Chapter 10.10: Preparation of Diols and Pinacol Rearrangement
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JoVE Core Organic Chemistry Chapter 10.11: Conversion of Alcohols to Alkyl Halides
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JoVE Core Organic Chemistry Chapter 10.12: Oxidation of Alcohols

챕터 0: Ethers, Epoxides, Sulfides

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JoVE Core Organic Chemistry Chapter 11.1: Structure and Nomenclature of Ethers
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JoVE Core Organic Chemistry Chapter 11.2: Physical Properties of Ethers
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JoVE Core Organic Chemistry Chapter 11.3: Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis
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JoVE Core Organic Chemistry Chapter 11.4: Ethers from Alkenes: Alcohol Addition and Alkoxymercuration-Demercuration
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JoVE Core Organic Chemistry Chapter 11.5: Ethers to Alkyl Halides: Acidic Cleavage
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JoVE Core Organic Chemistry Chapter 11.6: Autoxidation of Ethers to Peroxides and Hydroperoxides
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JoVE Core Organic Chemistry Chapter 11.7: Crown Ethers
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JoVE Core Organic Chemistry Chapter 11.8: Structure and Nomenclature of Epoxides
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JoVE Core Organic Chemistry Chapter 11.9: Preparation of Epoxides
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JoVE Core Organic Chemistry Chapter 11.10: Sharpless Epoxidation
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JoVE Core Organic Chemistry Chapter 11.11: Acid-Catalyzed Ring-Opening of Epoxides
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JoVE Core Organic Chemistry Chapter 11.12: Base-Catalyzed Ring-Opening of Epoxides
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JoVE Core Organic Chemistry Chapter 11.13: Structure and Nomenclature of Thiols and Sulfides
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JoVE Core Organic Chemistry Chapter 11.14: Preparation and Reactions of Thiols
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JoVE Core Organic Chemistry Chapter 11.15: Preparation and Reactions of Sulfides

챕터 0: Aldehydes and Ketones

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JoVE Core Organic Chemistry Chapter 12.1: Structures of Aldehydes and Ketones
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JoVE Core Organic Chemistry Chapter 12.2: IUPAC Nomenclature of Aldehydes
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JoVE Core Organic Chemistry Chapter 12.3: IUPAC Nomenclature of Ketones
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JoVE Core Organic Chemistry Chapter 12.4: Common Names of Aldehydes and Ketones
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JoVE Core Organic Chemistry Chapter 12.5: IR and UV–Vis Spectroscopy of Aldehydes and Ketones
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JoVE Core Organic Chemistry Chapter 12.6: NMR Spectroscopy and Mass Spectrometry of Aldehydes and Ketones
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JoVE Core Organic Chemistry Chapter 12.7: Preparation of Aldehydes and Ketones from Alcohols, Alkenes, and Alkynes
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JoVE Core Organic Chemistry Chapter 12.8: Preparation of Aldehydes and Ketones from Nitriles and Carboxylic Acids
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JoVE Core Organic Chemistry Chapter 12.9: Preparation of Aldehydes and Ketones from Carboxylic Acid Derivatives
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JoVE Core Organic Chemistry Chapter 12.10: Nucleophilic Addition to the Carbonyl Group: General Mechanism
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JoVE Core Organic Chemistry Chapter 12.11: Aldehydes and Ketones with Water: Hydrate Formation
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JoVE Core Organic Chemistry Chapter 12.12: Aldehydes and Ketones with Alcohols: Hemiacetal Formation
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JoVE Core Organic Chemistry Chapter 12.13: Protecting Groups for Aldehydes and Ketones: Introduction
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JoVE Core Organic Chemistry Chapter 12.14: Acetals and Thioacetals as Protecting Groups for Aldehydes and Ketones
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JoVE Core Organic Chemistry Chapter 12.15: Aldehydes and Ketones with HCN: Cyanohydrin Formation Overview
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JoVE Core Organic Chemistry Chapter 12.16: Aldehydes and Ketones with HCN: Cyanohydrin Formation Mechanism
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JoVE Core Organic Chemistry Chapter 12.17: Aldehydes and Ketones to Alkenes: Wittig Reaction Overview
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JoVE Core Organic Chemistry Chapter 12.18: Aldehydes and Ketones to Alkenes: Wittig Reaction Mechanism
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JoVE Core Organic Chemistry Chapter 12.19: Aldehydes and Ketones with Amines: Imine and Enamine Formation Overview
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JoVE Core Organic Chemistry Chapter 12.20: Aldehydes and Ketones with Amines: Imine Formation Mechanism
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JoVE Core Organic Chemistry Chapter 12.21: Aldehydes and Ketones with Amines: Enamine Formation Mechanism
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JoVE Core Organic Chemistry Chapter 12.22: Aldehydes and Ketones to Alkanes: Wolff–Kishner Reduction
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JoVE Core Organic Chemistry Chapter 12.23: Oxidations of Aldehydes and Ketones to Carboxylic Acids
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JoVE Core Organic Chemistry Chapter 12.24: Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation
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JoVE Core Organic Chemistry Chapter 12.25: Keto–Enol Tautomerism: Mechanism

챕터 0: Carboxylic Acids

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JoVE Core Organic Chemistry Chapter 13.1: IUPAC Nomenclature of Carboxylic Acids
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JoVE Core Organic Chemistry Chapter 13.2: Physical Properties of Carboxylic Acids
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JoVE Core Organic Chemistry Chapter 13.3: Acidity of Carboxylic Acids
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JoVE Core Organic Chemistry Chapter 13.4: Substituent Effects on Acidity of Carboxylic Acids
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JoVE Core Organic Chemistry Chapter 13.5: IR and UV–Vis Spectroscopy of Carboxylic Acids
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JoVE Core Organic Chemistry Chapter 13.6: NMR and Mass Spectroscopy of Carboxylic Acids
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JoVE Core Organic Chemistry Chapter 13.7: Preparation of Carboxylic Acids: Overview
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JoVE Core Organic Chemistry Chapter 13.8: Preparation of Carboxylic Acids: Hydrolysis of Nitriles
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JoVE Core Organic Chemistry Chapter 13.9: Preparation of Carboxylic Acids: Carboxylation of Grignard Reagents
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JoVE Core Organic Chemistry Chapter 13.10: Reactions of Carboxylic Acids: Introduction
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JoVE Core Organic Chemistry Chapter 13.11: Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
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JoVE Core Organic Chemistry Chapter 13.12: Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
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JoVE Core Organic Chemistry Chapter 13.13: Carboxylic Acids to Methylesters: Alkylation using Diazomethane
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JoVE Core Organic Chemistry Chapter 13.14: Carboxylic Acids to Acid Chlorides
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JoVE Core Organic Chemistry Chapter 13.15: Carboxylic Acids to Primary Alcohols: Hydride Reduction
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JoVE Core Organic Chemistry Chapter 13.16: Loss of Carboxy Group as CO2: Decarboxylation of β-Ketoacids
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JoVE Core Organic Chemistry Chapter 13.17: Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives

챕터 0: Carboxylic Acid Derivatives

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JoVE Core Organic Chemistry Chapter 14.1: Carboxylic Acid Derivatives: Overview
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JoVE Core Organic Chemistry Chapter 14.2: Nomenclature of Carboxylic Acid Derivatives: Acid Halides, Esters, and Acid Anhydrides
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JoVE Core Organic Chemistry Chapter 14.3: Nomenclature of Carboxylic Acid Derivatives: Amides and Nitriles
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JoVE Core Organic Chemistry Chapter 14.4: Structures of Carboxylic Acid Derivatives
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JoVE Core Organic Chemistry Chapter 14.5: Physical Properties of Carboxylic Acid Derivatives
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JoVE Core Organic Chemistry Chapter 14.6: Acidity and Basicity of Carboxylic Acid Derivatives
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JoVE Core Organic Chemistry Chapter 14.7: Spectroscopy of Carboxylic Acid Derivatives
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JoVE Core Organic Chemistry Chapter 14.8: Relative Reactivity of Carboxylic Acid Derivatives
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JoVE Core Organic Chemistry Chapter 14.9: Nucleophilic Acyl Substitution of Carboxylic Acid Derivatives
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JoVE Core Organic Chemistry Chapter 14.10: Acid Halides to Carboxylic Acids: Hydrolysis
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JoVE Core Organic Chemistry Chapter 14.11: Acid Halides to Esters: Alcoholysis
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JoVE Core Organic Chemistry Chapter 14.12: Acid Halides to Amides: Aminolysis
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JoVE Core Organic Chemistry Chapter 14.13: Acid Halides to Alcohols: LiAlH4 Reduction
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JoVE Core Organic Chemistry Chapter 14.14: Acid Halides to Alcohols: Grignard Reaction
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JoVE Core Organic Chemistry Chapter 14.15: Acid Halides to Ketones: Gilman Reagent
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JoVE Core Organic Chemistry Chapter 14.16: Preparation of Acid Anhydrides
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JoVE Core Organic Chemistry Chapter 14.17: Reactions of Acid Anhydrides
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JoVE Core Organic Chemistry Chapter 14.18: Esters to Carboxylic Acids: Saponification
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JoVE Core Organic Chemistry Chapter 14.19: Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
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JoVE Core Organic Chemistry Chapter 14.20: Esters to Alcohols: Hydride Reductions
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JoVE Core Organic Chemistry Chapter 14.21: Esters to Alcohols: Grignard Reaction
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JoVE Core Organic Chemistry Chapter 14.22: Preparation of Amides
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JoVE Core Organic Chemistry Chapter 14.23: Amides to Carboxylic Acids: Hydrolysis
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JoVE Core Organic Chemistry Chapter 14.24: Amides to Amines: LiAlH4 Reduction
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JoVE Core Organic Chemistry Chapter 14.25: Preparation of Nitriles
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JoVE Core Organic Chemistry Chapter 14.26: Nitriles to Carboxylic Acids: Hydrolysis
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JoVE Core Organic Chemistry Chapter 14.27: Nitriles to Ketones: Grignard Reaction
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JoVE Core Organic Chemistry Chapter 14.28: Nitriles to Amines: LiAlH4 Reduction

챕터 0: α-Carbon Chemistry: Enols, Enolates, and Enamines

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JoVE Core Organic Chemistry Chapter 15.1: Reactivity of Enols
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JoVE Core Organic Chemistry Chapter 15.2: Reactivity of Enolate Ions
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JoVE Core Organic Chemistry Chapter 15.3: Types of Enols and Enolates
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JoVE Core Organic Chemistry Chapter 15.4: Enolate Mechanism Conventions
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JoVE Core Organic Chemistry Chapter 15.5: Regioselective Formation of Enolates
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JoVE Core Organic Chemistry Chapter 15.6: Stereochemical Effects of Enolization
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JoVE Core Organic Chemistry Chapter 15.7: Acid-Catalyzed α-Halogenation of Aldehydes and Ketones
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JoVE Core Organic Chemistry Chapter 15.8: Base-Promoted α-Halogenation of Aldehydes and Ketones
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JoVE Core Organic Chemistry Chapter 15.9: Multiple Halogenation of Methyl Ketones: Haloform Reaction
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JoVE Core Organic Chemistry Chapter 15.10: α-Halogenation of Carboxylic Acid Derivatives: Overview
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JoVE Core Organic Chemistry Chapter 15.11: α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction
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JoVE Core Organic Chemistry Chapter 15.12: Reactions of α-Halocarbonyl Compounds: Nucleophilic Substitution
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JoVE Core Organic Chemistry Chapter 15.13: Nitrosation of Enols
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JoVE Core Organic Chemistry Chapter 15.14: C–C Bond Formation: Aldol Condensation Overview
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JoVE Core Organic Chemistry Chapter 15.15: Base-Catalyzed Aldol Addition Reaction
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JoVE Core Organic Chemistry Chapter 15.16: Acid-Catalyzed Aldol Addition Reaction
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JoVE Core Organic Chemistry Chapter 15.17: Dehydration of Aldols to Enals: Base-Catalyzed Aldol Condensation
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JoVE Core Organic Chemistry Chapter 15.18: Dehydration of Aldols to Enones: Acid-Catalyzed Aldol Condensation
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JoVE Core Organic Chemistry Chapter 15.19: Intramolecular Aldol Reaction
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JoVE Core Organic Chemistry Chapter 15.20: C–C Bond Cleavage: Retro-Aldol Reaction
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JoVE Core Organic Chemistry Chapter 15.21: Crossed Aldol Reactions: Overview
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JoVE Core Organic Chemistry Chapter 15.22: Crossed Aldol Reaction Using Weak Bases
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JoVE Core Organic Chemistry Chapter 15.23: Ketones with Nonenolizable Aromatic Aldehydes: Claisen–Schmidt Condensation
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JoVE Core Organic Chemistry Chapter 15.24: Crossed Aldol Reaction Using Strong Bases: Directed Aldol Reaction
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JoVE Core Organic Chemistry Chapter 15.25: Aldol Condensation with β-Diesters: Knoevenagel Condensation
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JoVE Core Organic Chemistry Chapter 15.26: Esters to β-Ketoesters: Claisen Condensation Overview
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JoVE Core Organic Chemistry Chapter 15.27: Esters to β-Ketoesters: Claisen Condensation Mechanism
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JoVE Core Organic Chemistry Chapter 15.28: Aldol Condensation vs Claisen Condensation
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JoVE Core Organic Chemistry Chapter 15.29: Intramolecular Claisen Condensation of Dicarboxylic Esters: Dieckmann Cyclization
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JoVE Core Organic Chemistry Chapter 15.30: β-Dicarbonyl Compounds via Crossed Claisen Condensations
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JoVE Core Organic Chemistry Chapter 15.31: α-Alkylation of Ketones via Enolate Ions
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JoVE Core Organic Chemistry Chapter 15.32: Factors Affecting α-Alkylation of Ketones: Choice of Base
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JoVE Core Organic Chemistry Chapter 15.33: Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
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JoVE Core Organic Chemistry Chapter 15.34: Alkylation of β-Diester Enolates: Malonic Ester Synthesis
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JoVE Core Organic Chemistry Chapter 15.35: Conjugate Addition to α,β-Unsaturated Carbonyl Compounds
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JoVE Core Organic Chemistry Chapter 15.36: Conjugate Addition (1,4-Addition) vs Direct Addition (1,2-Addition)
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JoVE Core Organic Chemistry Chapter 15.37: Conjugate Addition of Enolates: Michael Addition
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JoVE Core Organic Chemistry Chapter 15.38: Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation
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JoVE Core Organic Chemistry Chapter 15.39: Synthesis of α-Substituted Carbonyl Compounds: The Stork Enamine Reaction
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JoVE Core Organic Chemistry Chapter 15.40: Nonenolizable Aldehydes to Acids and Alcohols: The Cannizzaro Reaction

챕터 0: Dienes, Conjugated Pi Systems, and Pericyclic Reactions

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JoVE Core Organic Chemistry Chapter 16.1: Structure of Conjugated Dienes
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JoVE Core Organic Chemistry Chapter 16.2: Stability of Conjugated Dienes
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JoVE Core Organic Chemistry Chapter 16.3: π Molecular Orbitals of 1,3-Butadiene
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JoVE Core Organic Chemistry Chapter 16.4: π Molecular Orbitals of the Allyl Cation and Anion
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JoVE Core Organic Chemistry Chapter 16.5: π Molecular Orbitals of the Allyl Radical
30
JoVE Core Organic Chemistry Chapter 16.6: Electrophilic 1,2- and 1,4-Addition of HX to 1,3-Butadiene
30
JoVE Core Organic Chemistry Chapter 16.7: Electrophilic 1,2- and 1,4-Addition of X2 to 1,3-Butadiene
30
JoVE Core Organic Chemistry Chapter 16.8: Electrophilic Addition of HX to 1,3-Butadiene: Thermodynamic vs Kinetic Control
30
JoVE Core Organic Chemistry Chapter 16.9: UV–Vis Spectroscopy of Conjugated Systems
30
JoVE Core Organic Chemistry Chapter 16.10: UV–Vis Spectroscopy: Woodward–Fieser Rules
30
JoVE Core Organic Chemistry Chapter 16.11: Pericyclic Reactions: Introduction
30
JoVE Core Organic Chemistry Chapter 16.12: Thermal and Photochemical Electrocyclic Reactions: Overview
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JoVE Core Organic Chemistry Chapter 16.13: Thermal Electrocyclic Reactions: Stereochemistry
30
JoVE Core Organic Chemistry Chapter 16.14: Photochemical Electrocyclic Reactions: Stereochemistry
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JoVE Core Organic Chemistry Chapter 16.15: Cycloaddition Reactions: Overview
30
JoVE Core Organic Chemistry Chapter 16.16: Cycloaddition Reactions: MO Requirements for Thermal Activation
30
JoVE Core Organic Chemistry Chapter 16.17: Cycloaddition Reactions: MO Requirements for Photochemical Activation
30
JoVE Core Organic Chemistry Chapter 16.18: [4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
30
JoVE Core Organic Chemistry Chapter 16.19: Diels–Alder vs Retro-Diels–Alder Reaction: Thermodynamic Factors
30
JoVE Core Organic Chemistry Chapter 16.20: Diels–Alder Reaction Forming Cyclic Products: Stereochemistry
30
JoVE Core Organic Chemistry Chapter 16.21: Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry
30
JoVE Core Organic Chemistry Chapter 16.22: Diels–Alder Reaction: Characteristics of Dienes
30
JoVE Core Organic Chemistry Chapter 16.23: Diels–Alder Reaction: Characteristics of Dienophiles
30
JoVE Core Organic Chemistry Chapter 16.24: Thermal Sigmatropic Reactions: Overview
30
JoVE Core Organic Chemistry Chapter 16.25: [3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement
30
JoVE Core Organic Chemistry Chapter 16.26: [3,3] Sigmatropic Rearrangement of Allyl Vinyl Ethers: Claisen Rearrangement
30
JoVE Core Organic Chemistry Chapter 16.27: Woodward–Hoffmann Selection Rules and Microscopic Reversibility

챕터 0: Aromatic Compounds

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JoVE Core Organic Chemistry Chapter 17.1: Aromatic Compounds: Overview
30
JoVE Core Organic Chemistry Chapter 17.2: Nomenclature of Aromatic Compounds with a Single Substituent
30
JoVE Core Organic Chemistry Chapter 17.3: Nomenclature of Aromatic Compounds with Multiple Substituents
30
JoVE Core Organic Chemistry Chapter 17.4: Structure of Benzene: Kekulé Model
30
JoVE Core Organic Chemistry Chapter 17.5: Structure of Benzene: Molecular Orbital Model
30
JoVE Core Organic Chemistry Chapter 17.7: Criteria for Aromaticity and the Hückel 4n + 2 Rule
30
JoVE Core Organic Chemistry Chapter 17.8: Hückel's Rule Diagram of π MOs: Frost Circle
30
JoVE Core Organic Chemistry Chapter 17.9: Frost Circles for Different Conjugated Systems
30
JoVE Core Organic Chemistry Chapter 17.13: Aromatic Hydrocarbon Anions: Structural Overview
30
JoVE Core Organic Chemistry Chapter 17.14: Aromatic Hydrocarbon Cations: Structural Overview
30
JoVE Core Organic Chemistry Chapter 17.15: Five-Membered Heterocyclic Aromatic Compounds: Overview
30
JoVE Core Organic Chemistry Chapter 17.19: NMR Spectroscopy of Aromatic Compounds

챕터 0: Reactions of Aromatic Compounds

30
JoVE Core Organic Chemistry Chapter 18.4: NMR Spectroscopy of Benzene Derivatives
30
JoVE Core Organic Chemistry Chapter 18.5: Reactions at the Benzylic Position: Oxidation and Reduction
30
JoVE Core Organic Chemistry Chapter 18.7: Reactions at the Benzylic Position: Halogenation
30
JoVE Core Organic Chemistry Chapter 18.8: Electrophilic Aromatic Substitution: Overview
30
JoVE Core Organic Chemistry Chapter 18.9: Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene
30
JoVE Core Organic Chemistry Chapter 18.10: Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
30
JoVE Core Organic Chemistry Chapter 18.11: Electrophilic Aromatic Substitution: Nitration of Benzene
30
JoVE Core Organic Chemistry Chapter 18.12: Electrophilic Aromatic Substitution: Sulfonation of Benzene
30
JoVE Core Organic Chemistry Chapter 18.13: Electrophilic Aromatic Substitution: Friedel–Crafts Alkylation of Benzene
30
JoVE Core Organic Chemistry Chapter 18.14: Electrophilic Aromatic Substitution: Friedel–Crafts Acylation of Benzene
30
JoVE Core Organic Chemistry Chapter 18.15: Limitations of Friedel–Crafts Reactions
30
JoVE Core Organic Chemistry Chapter 18.16: Directing Effect of Substituents: ortho–para-Directing Groups
30
JoVE Core Organic Chemistry Chapter 18.17: Directing Effect of Substituents: meta-Directing Groups
30
JoVE Core Organic Chemistry Chapter 18.18: ortho–para-Directing Activators: –CH3, –OH, –⁠NH2, –OCH3
30
JoVE Core Organic Chemistry Chapter 18.19: ortho–para-Directing Deactivators: Halogens
30
JoVE Core Organic Chemistry Chapter 18.20: meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H
30
JoVE Core Organic Chemistry Chapter 18.21: Directing and Steric Effects in Disubstituted Benzene Derivatives
30
JoVE Core Organic Chemistry Chapter 18.23: Nucleophilic Aromatic Substitution: Addition–Elimination (SNAr)
30
JoVE Core Organic Chemistry Chapter 18.24: Nucleophilic Aromatic Substitution: Elimination–Addition
30
JoVE Core Organic Chemistry Chapter 18.25: Nucleophilic Aromatic Substitution of Aryldiazonium Salts: Aromatic SN1
30
JoVE Core Organic Chemistry Chapter 18.26: Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
30
JoVE Core Organic Chemistry Chapter 18.28: Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism
30
JoVE Core Organic Chemistry Chapter 18.29: Hydrolysis of Chlorobenzene to Phenol: Dow Process
30
JoVE Core Organic Chemistry Chapter 18.30: Benzene to Phenol via Cumene: Hock Process
30
JoVE Core Organic Chemistry Chapter 18.32: Oxidation of Phenols to Quinones

챕터 0: Amines

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JoVE Core Organic Chemistry Chapter 19.1: Amines: Introduction
30
JoVE Core Organic Chemistry Chapter 19.2: Nomenclature of Primary Amines
30
JoVE Core Organic Chemistry Chapter 19.3: Nomenclature of Secondary and Tertiary Amines
30
JoVE Core Organic Chemistry Chapter 19.4: Nomenclature of Aryl and Heterocyclic Amines
30
JoVE Core Organic Chemistry Chapter 19.5: Structure of Amines
30
JoVE Core Organic Chemistry Chapter 19.6: Physical Properties of Amines
30
JoVE Core Organic Chemistry Chapter 19.7: Basicity of Aliphatic Amines
30
JoVE Core Organic Chemistry Chapter 19.8: Basicity of Aromatic Amines
30
JoVE Core Organic Chemistry Chapter 19.9: Basicity of Heterocyclic Aromatic Amines
30
JoVE Core Organic Chemistry Chapter 19.10: NMR Spectroscopy Of Amines
30
JoVE Core Organic Chemistry Chapter 19.12: Mass Spectrometry of Amines
30
JoVE Core Organic Chemistry Chapter 19.13: Preparation of Amines: Alkylation of Ammonia and Amines
30
JoVE Core Organic Chemistry Chapter 19.14: Preparation of 1° Amines: Azide Synthesis
30
JoVE Core Organic Chemistry Chapter 19.15: Preparation of 1° Amines: Gabriel Synthesis
30
JoVE Core Organic Chemistry Chapter 19.16: Preparation of Amines: Reduction of Oximes and Nitro Compounds
30
JoVE Core Organic Chemistry Chapter 19.17: Preparation of Amines: Reduction of Amides and Nitriles
30
JoVE Core Organic Chemistry Chapter 19.18: Preparation of Amines: Reductive Amination of Aldehydes and Ketones
30
JoVE Core Organic Chemistry Chapter 19.19: Preparation of 1° Amines: Hofmann and Curtius Rearrangement Overview
30
JoVE Core Organic Chemistry Chapter 19.20: Preparation of 1° Amines: Hofmann and Curtius Rearrangement Mechanism
30
JoVE Core Organic Chemistry Chapter 19.21: Amines to Amides: Acylation of Amines
30
JoVE Core Organic Chemistry Chapter 19.22: Amines to Alkenes: Hofmann Elimination
30
JoVE Core Organic Chemistry Chapter 19.24: Amines to Alkenes: Cope Elimination
30
JoVE Core Organic Chemistry Chapter 19.25: 1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
30
JoVE Core Organic Chemistry Chapter 19.26: 1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
30
JoVE Core Organic Chemistry Chapter 19.27: 2° Amines to N-Nitrosamines: Reaction with NaNO2
30
JoVE Core Organic Chemistry Chapter 19.28: Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions
30
JoVE Core Organic Chemistry Chapter 19.29: Diazonium Group Substitution: –OH and –H
30
JoVE Core Organic Chemistry Chapter 19.30: Aryldiazonium Salts to Azo Dyes: Diazo Coupling
30
JoVE Core Organic Chemistry Chapter 19.31: Amines to Sulfonamides: The Hinsberg Test

챕터 0: Radical Chemistry

30
JoVE Core Organic Chemistry Chapter 20.1: Radicals: Electronic Structure and Geometry
30
JoVE Core Organic Chemistry Chapter 20.4: Electron Paramagnetic Resonance (EPR) Spectroscopy: Organic Radicals
30
JoVE Core Organic Chemistry Chapter 20.5: Radical Formation: Overview
30
JoVE Core Organic Chemistry Chapter 20.6: Radical Formation: Homolysis
30
JoVE Core Organic Chemistry Chapter 20.7: Radical Formation: Abstraction
30
JoVE Core Organic Chemistry Chapter 20.8: Radical Formation: Addition
30
JoVE Core Organic Chemistry Chapter 20.9: Radical Formation: Elimination
30
JoVE Core Organic Chemistry Chapter 20.10: Radical Reactivity: Overview
30
JoVE Core Organic Chemistry Chapter 20.11: Radical Reactivity: Steric Effects
30
JoVE Core Organic Chemistry Chapter 20.12: Radical Reactivity: Concentration Effects
30
JoVE Core Organic Chemistry Chapter 20.13: Radical Reactivity: Electrophilic Radicals
30
JoVE Core Organic Chemistry Chapter 20.14: Radical Reactivity: Nucleophilic Radicals
30
JoVE Core Organic Chemistry Chapter 20.15: Radical Reactivity: Intramolecular vs Intermolecular
30
JoVE Core Organic Chemistry Chapter 20.16: Radical Autoxidation
30
JoVE Core Organic Chemistry Chapter 20.17: Radical Oxidation of Allylic and Benzylic Alcohols
30
JoVE Core Organic Chemistry Chapter 20.18: Radical Substitution: Halogenation of Alkanes and Alkyl Substituents
30
JoVE Core Organic Chemistry Chapter 20.19: Radical Halogenation: Thermodynamics
30
JoVE Core Organic Chemistry Chapter 20.21: Radical Halogenation: Stereochemistry
30
JoVE Core Organic Chemistry Chapter 20.22: Radical Substitution: Allylic Chlorination
30
JoVE Core Organic Chemistry Chapter 20.23: Radical Substitution: Allylic Bromination
30
JoVE Core Organic Chemistry Chapter 20.24: Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
30
JoVE Core Organic Chemistry Chapter 20.25: Radical Anti-Markovnikov Addition to Alkenes: Overview
30
JoVE Core Organic Chemistry Chapter 20.26: Radical Anti-Markovnikov Addition to Alkenes: Mechanism
30
JoVE Core Organic Chemistry Chapter 20.27: Radical Anti-Markovnikov Addition to Alkenes: Thermodynamics
30
JoVE Core Organic Chemistry Chapter 20.28: Vicinal Diols via Reductive Coupling of Aldehydes or Ketones: Pinacol Coupling Overview
30
JoVE Core Organic Chemistry Chapter 20.30: Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction
30
JoVE Core Organic Chemistry Chapter 20.31: α-Hydroxy Ketones via Reductive Coupling of Esters: Acyloin Condensation Overview

챕터 0: Synthetic Polymers

30
JoVE Core Organic Chemistry Chapter 21.2: Characteristics and Nomenclature of Homopolymers
30
JoVE Core Organic Chemistry Chapter 21.3: Characteristics and Nomenclature of Copolymers
30
JoVE Core Organic Chemistry Chapter 21.4: Polymers: Defining Molecular Weight
30
JoVE Core Organic Chemistry Chapter 21.5: Polymers: Molecular Weight Distribution
30
JoVE Core Organic Chemistry Chapter 21.6: Polymer Classification: Architecture
30
JoVE Core Organic Chemistry Chapter 21.7: Polymer Classification: Crystallinity
30
JoVE Core Organic Chemistry Chapter 21.8: Polymer Classification: Stereospecificity
30
JoVE Core Organic Chemistry Chapter 21.10: Radical Chain-Growth Polymerization: Overview
30
JoVE Core Organic Chemistry Chapter 21.11: Radical Chain-Growth Polymerization: Mechanism
30
JoVE Core Organic Chemistry Chapter 21.12: Radical Chain-Growth Polymerization: Chain Branching
30
JoVE Core Organic Chemistry Chapter 21.13: Anionic Chain-Growth Polymerization: Overview
30
JoVE Core Organic Chemistry Chapter 21.14: Anionic Chain-Growth Polymerization: Mechanism
30
JoVE Core Organic Chemistry Chapter 21.16: Cationic Chain-Growth Polymerization: Mechanism
30
JoVE Core Organic Chemistry Chapter 21.17: Ziegler–Natta Chain-Growth Polymerization: Overview
30
JoVE Core Organic Chemistry Chapter 21.19: Step-Growth Polymerization: Overview
30
JoVE Core Organic Chemistry Chapter 21.20: Molecular Weight of Step-Growth Polymers
30
JoVE Core Organic Chemistry Chapter 21.22: Types of Step-Growth Polymers: Polyesters
30
JoVE Core Organic Chemistry Chapter 21.24: Olefin Metathesis Polymerization: Overview
30
JoVE Core Organic Chemistry Chapter 21.25: Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
30
JoVE Core Organic Chemistry Chapter 21.26: Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

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JoVE Core
Organic Chemistry

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대체 사이클로헥산의 안정성

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이전 동영상
JoVE Core Organic Chemistry Chapter 3.11: 사이클로헥산의 의자 형태

다음 비디오
JoVE Core Organic Chemistry Chapter 3.13: 디대체 사이클로헥산: 시스 트랜스 이소머리즘

임베드 Languages 즐겨찾기에 추가 플레이리스트에 추가

스크립트

평형에서 사이클로헥산의 두 의자 순응은 동일한 에너지와 불안정을 가지고 있으며, 각 원포는 평형 혼합물의 약 50 %를 나타냅니다.

수소 원자를 알킬 그룹으로 교체하면 두 개의 적합성이 정력적으로 비등합니다.

예를 들어, 메틸시클로헥산에서 CH₃ 그룹은 하나의 의자 형태와 다른 사람의 적도 위치에서 축 위치를 차지합니다.

축 형성은 적도 형성에 비해 약 7.6 kJ mol^-1의 높은 에너지를 가지고, 후자를 더 안정적으로.

따라서, 적도 형성은 평형 혼합물의 약 95%를 포함한다. 문제는 에너지와 안정성의 이러한 변화의 이유는 무엇인가?

연구에 따르면 축 형성에서 메틸 수소는 링의 동일한 쪽에 두 개의 병렬 및 밀접하게 배치된 축 수소를 가진 반발 분산 상호 작용을 경험합니다.

C1과 C3 또는 C5에 있는 단 사이 이 불리한 steric 긴장은 1,3-diaxial 상호 작용이라고 합니다, 이는 gauche 상호 작용입니다.

각 고슈 상호 작용은 약 3.8 kJ의 추가 에너지를 기여합니다.

이러한 고슈 상호 작용은 메틸 그룹이 C3 및 C5에 반대로 배치되기 때문에 적도 형성에 결석한다. 따라서, 메틸 사이클로헥산의 분자는 주로 낮은 에너지, 더 안정적인 적도 형태를 채택한다.

단조로대체 사이클로알케인에서는 대체체의 크기가 증가함에 따라 1,3-투이질 상호 작용이 강해져 두 적합성 간의 에너지 차이가 더욱 두드러집니다.

이것은 대체가 tert-butyl단일 때 특히 분명합니다. 저에너지 적도 형성은 축 형성보다 훨씬 더 안정적이며 99 %가 풍부합니다.

디메틸 사이클로헥산과 같이 대체된 사이클클로알카네인에서는 메틸 그룹 간의 비질 반발이 증가하여 분자의 축 형성 확률을 더욱 감소시킵니다.

JoVE Core Organic Chemistry Chapter 3.12: 대체 사이클로헥산의 안정성

이 단원에서는 다양한 순응자의 에너지와 1,3-diaxial 상호 작용의 효과에 중점을 둔 대체 사이클로헥산의 안정성에 대해 설명합니다.

사이클로헥산의 두 의자 적합성은 실온에서 급속한 상호 변환을 겪습니다. 두 형태 모두 동일한 에너지와 불안정을 가지며, 각각 평형 혼합물의 동일한 양을 포함합니다. 수소 원자를 기능성 그룹으로 교체하면 두 개의 적합성이 정력적으로 비등합니다.

예를 들어, 메틸사이클로헥산에서 CH₃ 그룹은 하나의 의자 형태와 다른 의자 형태에서 적도 위치를 차지한다. 이것은 약 7.6 kJ mol^-1에축 축 형태의 에너지의 증가로 이끌어 내고, 적도 형성을 95%의 풍부하게 보다 안정적으로 만듭니다.

에너지와 안정성의 이러한 변화에 대한 이유는 메틸 수소가 링의 동일한 쪽에 두 개의 평행및 밀접하게 배치 된 축 수소를 가진 반발 분산 상호 작용을 경험하기 때문입니다. steric 균주는 C1과 C3 또는 C5에 있는 단 사이에서 유래하기 때문에, 1,3-투진 상호 작용이라고 합니다. 이러한 상호 작용은 뉴먼 프로젝션과 함께 표시되면 고슈 관계를 나타낸다. 그러나, 메틸 그룹이 적도에 위치하는 경우, 그것은 Steric 반발을 최소화, C3 및 C5에 반대로 배치된다.

기능성 그룹의 크기가 증가함에 따라 1,3-투이질 상호 작용이 더욱 두드러지므로 두 적합성 간의 에너지 차이가 증가합니다.

챕터 0: 공유결합과 구조

챕터 0: 열역학과 화학반응속도론

챕터 0: 알케인과 사이클로알케인

챕터 0: 입체 이성질

챕터 0: 산과 염기

챕터 0: 친핵성 치환과 알킬 할라이드 반응 제거

챕터 0: Alkene Structure and Reactivity

챕터 0: Reactions of Alkenes

챕터 0: Alkynes

챕터 0: Alcohols and Phenols

챕터 0: Ethers, Epoxides, Sulfides

챕터 0: Aldehydes and Ketones

챕터 0: Carboxylic Acids

챕터 0: Carboxylic Acid Derivatives

챕터 0: α-Carbon Chemistry: Enols, Enolates, and Enamines

챕터 0: Dienes, Conjugated Pi Systems, and Pericyclic Reactions

챕터 0: Aromatic Compounds

챕터 0: Reactions of Aromatic Compounds

챕터 0: Amines

챕터 0: Radical Chemistry

챕터 0: Synthetic Polymers

JoVE Core Organic Chemistry Chapter 3.12: 대체 사이클로헥산의 안정성

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