Ammonia Addition

Ammonia addition is the controlled introduction of ammonia (NH₃) into a chemical system to alter its composition, acidity, or reactivity. In aqueous solutions, ammonia acts as a weak Brønsted base, accepting protons to form ammonium and hydroxide ions, while also coordinating with metal ions to produce soluble ammine complexes; the outcome depends on concentration, pH, temperature, and mixing. Chemists use ammonia addition in acid–base studies, qualitative analysis, precipitation control, coordination chemistry, and chemical synthesis. Careful control of the addition rate and amount helps regulate reaction conditions, improve selectivity, and interpret changes in solution color, solubility, or composition.

Ammonia Addition - Related Videos

Research

JoVE Journal - Bioengineering

Ammonia Synthesis at Low Pressure

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Cited by 17 •

2017

Ammonia can be synthesized at low pressure by using a conventional catalyst and an ammonia selective absorbent.

Fast and Accurate Exhaled Breath Ammonia Measurement

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Cited by 16 •

2014

Ammonia is an important physiologic metabolite relevant to various disease and wellness states. It is also a difficult molecule to measure in breath, which demands particular precautions be taken to obtain accurate results. Not all factors influencing ammonia are known, but progress can be difficult without accounting for these factors.

Education

JoVE Core - Organic Chemistry

Conjugate Addition (1,4-Addition) vs Direct Addition (1,2-Addition)

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2025

α,β-Unsaturated carbonyl compounds with two electrophilic sites, the carbonyl carbon, and the β carbon, are susceptible to nucleophilic attack via two modes: conjugate or 1,4-addition and direct or 1,2-addition. Conjugate addition results in a thermodynamically stable product. The reaction retains the stronger C=O bond at the expense of the weaker C=C π bond. The process is slow as the β carbon is less electrophilic than the carbonyl carbon. Direct addition products are formed faster owing to...

Conjugate Addition of Enolates: Michael Addition

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2023

The attack of a nucleophile at the β carbon of an α,β-unsaturated carbonyl compound is called conjugate addition. Conjugate addition reactions of active methylene compounds, such as β-diketones, β-keto esters, β-keto nitriles, and α-nitro ketones, are called Michael addition reactions. The reaction is catalyzed by a base that abstracts the acidic methylene hydrogen, generating a doubly-stabilized enolate ion that serves as the nucleophile or the Michael donor. The base employed depends on the...

Preparation of Hydrophobic Metal-Organic Frameworks via Plasma Enhanced Chemical Vapor Deposition of Perfluoroalkanes for the Removal of Ammonia

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Cited by 15 •

2013

Herein the procedures for plasma enhanced chemical vapor deposition of perfluoroalkanes on microporous materials such as metal-organic frameworks to enhance their stability and hydrophobicity are described. Furthermore, breakthrough testing of milligram quantities of samples is described in detail.

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