Name: ph at key points in a weak acid titration
Uploaded: 2020-09-24T15:06:51.000Z
Duration: 3 min 55 s
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titration-calculations-weak-acid-strong-base

Titration Calculations: Weak Acid - Strong Base

قيمة pH عند المراحل المختلفة لمعايرة حمض أو قاعدة ضعيفين،تُحسب باستخدام طرق مختلفة خلال النقاط المختلفة لعملية المعايرة. إذا كان الحمض الضعيف أو القاعدة المُحدّد الرئيسي لقيمة pH،تُستخدم Ka أو Kb وجدول مراقبة التغير،أو تُستخدم معادلة هندرسون هاسلبالخ. إذا تواجد حمض قوي أو قاعدة بعد تفاعل التحييد،يُستخدم تركيز أيونات الهيدرونيوم أو الهيدروكسيد المتبقية لحساب قيمة pH.قيمة pH الأولية لـ50 مللتر من محلول حمض الخليك بتركيز 0.10 تساوي 2.87 وتُحسب باستخدام Ka وجدول مراقبة التغير ICE،لأن حمض الخليك هو المساهم الرئيسي. إذا جرت معايرة هذا المحلول الذي يحتوي على 0.0050 من الأسيتات مع هيدروكسيد الصوديوم بتركيز 0.10 مولار،تتفاعل أيونات الهيدروكسيد مع حمض الخليك لإنتاج الأسيتات،فينتج عن ذلك محلول منظّم. لذلك عند إضافة 10 مللتر من هيدروكسيد الصوديوم،تحتوي على 0.0010 مول من أيونات الهيدروكسيد،تتشكل 0.0010 مول من الأسيتات،وتبقى 0.0040 مول من حمض الخليك.يمكن حساب قيمة pH للمحلول المنظّم،باستبدال هذه القيم في معادلة هندرسون هاسلبالخ وتساوي 4.14. عند إضافة 25 مللتر من هيدروكسيد الصوديوم،يجري تحويل نصف مولات حمض الخليك الأولية إلى أسيتات. في هذه المرحلة تكون قيمة pH مساوية لقيمة pKa،لأن كمية أيونات حمض الخليك وأيونات الأسيتات متساوية.إضافة مزيد من هيدروكسيد الصوديوم لتصل إلى 50 مللتر،تحوّل جميع جزيئات حمض الخليك إلى أسيتات،ويتحقق الوصول إلى نقطة التكافؤ. بما أن أيونات الأسيتات قاعدية،فإن نقطة التكافؤ تقع في المنطقة القاعدية. يُحسب تركيز أيونات الأسيتات،بقسمة عدد المولات على كمية المحلول الإجمالية.تُحدد قيمة pH،باستخدام قيمة Kb لأيونات الأسيتات وجدول مراقبة التغيير ICE،لأن أيون الأسيتات هو المساهم الرئيسي في درجة pH عند نقطة التكافؤ. تُحسب قيمة Kb للأسيتات،باستخدام الصيغة:Kw تساوي Ka مضروبة في Kb وتساوي 5.6 10-¹. باستبدال قيم التركيز عند التوازن في معادلة Kb يعطي تركيز الهيدروكسيد،وتساوي 5.3 10⁻⁶ مولار.وتكون قيمة pOH وقيمة pH للمحلول 5.28 و 8.72،على التوالي. إضافة مزيد من هيدروكسيد الصوديوم إلى المحلول،تؤدي إلى خليط من أيونات الأسيتات وهيدروكسيد الصوديوم. إلّا أن التركيز النهائي لهيدروكسيد الصوديوم هو الذي يحدد قيمة pH للمحلول،لأنه قاعدة أقوى من الأسيتات.لذلك إذا أضيفت 70 مللتر من هيدروكسيد الصوديوم إلى المحلول،يمكن حساب التركيز النهائي لأيونات الهيدروكسيد بطرح العدد الإجمالي لمولات حمض الخليك،وهو 0.0050 مول من العدد الإجمالي لأيونات الهيدروكسيد وهو 0.0070،وقسمة الناتج على كمية المحلول الإجمالية،وهي 120 مللتر أو 0.12 لتر. بما أن تركيز أيونات الهيدروكسيد يساوي 0.017 مولار،تُحسب قيمة كل من pOH و PH للمحلول لتكون 1.78 و 12.22 على التوالي.

حسابات المعايرة: حمض ضعيف-قاعدة ضعيفة

حساب الرقم الهيدروجيني لحلول المعايرة: حمض ضعيف/قاعدة قوية لمعايرة 25.00 مل من 0.100 مول CH3CO2H، يمكن تمثيل التفاعل على النحو التالي: <img alt="Eq1" src="/files/ftp_upload/11414/11414_Equation_1.png" style="text-align: center; height: 50px;" /> يمكن حساب الرقم الهيدروجيني لمحلول المعايرة بعد إضافة الأحجام المختلفة من معاير NaOH على النحو التالي: (أ) يتم حساب الأس الهيدروجيني الأولي لمحلول حمض الأسيتيك في نهج ICE المعتاد: <img alt="Eq2" src="/files/ftp_upload/11414/11414_Equation_2.png" style="text-align: center; height: 155px;" /> (ب) يعتبر كل من الحمض والمعاير أحادي الخلية والعينة ومحاليل المعايرة مركزة بشكل متساوٍ؛ وبالتالي، يمثل هذا الحجم من المعاير نقطة التكافؤ. على عكس مثال الحمض القوي، يحتوي خليط التفاعل في هذه الحالة على قاعدة مترافقة ضعيفة (أيون الأسيتات). يتم حساب الرقم الهيدروجيني للمحلول مع الأخذ في الاعتبار التأين الأساسي للأسيتات ، والذي يوجد بتركيز <img alt="Eq3" src="/files/ftp_upload/11414/11414_Equation_3.png" style="text-align: center; height: 72px;" /> يتم تمثيل التأين الأساسي للأسيتات بالمعادلة <img alt="Eq4" src="/files/ftp_upload/11414/11414_Equation_4.png" style="text-align: center; height: 115px;" /> بافتراض x << 0.0500، يمكن حساب الأس الهيدروجيني من خلال نهج ICE المعتاد: <img alt="Eq5" src="/files/ftp_upload/11414/11414_Equation_5.png" style="text-align: center; height: 150px;" /> لاحظ أن الرقم الهيدروجيني عند نقطة التكافؤ لهذه المعايرة أكبر بكثير من 7، كما هو متوقع عند معايرة حمض ضعيف بقاعدة قوية. (ج) حجم المعاير = 12.50 مل. يمثل هذا الحجم نصف كمية القياس المتكافئ للمعايرة، وبالتالي تم تحييد نصف حمض الأسيتيك لإنتاج كمية مكافئة من أيون الأسيتات. وبالتالي، فإن تراكيز تلك الأزواج المتقارنة من حمض-قاعدة متساوية. من الأساليب الملائمة لحساب الرقم الهيدروجيني استخدام معادلة هندرسون-هاسلبالخ: <img alt="Eq6" src="/files/ftp_upload/11414/11414_Equation_6.png" style="text-align: center; height: 115px;" /> (pH = pKa عند نقطة نصف التكافؤ في معايرة حمض ضعيف) (د) حجم المعاير = 37.50 مل. يمثل هذا الحجم فائضاً في القياس المتكافئ للمعايرة، ومحلول تفاعل يحتوي على منتج المعايرة، وأيون الأسيتات، والمعايرة القوية الزائدة. في مثل هذه المحاليل، يتم تحديد الرقم الهيدروجيني للمحلول بشكل أساسي من خلال المقدار الزائد من القاعدة القوية: <img alt="Eq7" src="/files/ftp_upload/11414/11414_Equation_7.png" style="text-align: center; height: 155px;" />هذا النص مقتبس من<a href="https://openstax.org/books/chemistry-2e/pages/14-7-acid-base-titrations"> Openstax, Chemistry 2e, Section 14.7: Acid-base Titrations.</a>

حساب الأس الهيدروجيني لمحاليل المعايرة بالتحليل الحجمي: حمض ضعيف / قاعدة قوية
بالنسبة للمعايرة بالتحليل الحجمي 25.00 مل من 0.100 م CH3CO2H مع 0.100 M هيدروكسيد الصوديوم ، يمكن أن يكون التفاعل ...

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Acid-base and Solubility Equilibria

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ph at key points in a weak acid titration

pH at key points in a weak acid titration can be calculated for an acetic acid solution as sodium hydroxide is added. The example uses 25.00 mL of 0.100 M CH3CO2H titrated with 0.100 M NaOH. The reaction is shown as the weak acid reacts with the strong base.

The initial pH is found from the acetic acid solution using the usual ICE approach. ICE means initial, change, and equilibrium, and it is a common way to set up equilibrium problems. The solution pH is calculated before any titrant is added.

When 25.00 mL of NaOH has been added, the titration reaches the equivalence point. The acid and titrant are both monoprotic, and the sample and titrant have the same concentration. At this point, the mixture contains acetate ion, which is the weak conjugate base of acetic acid.

Because acetate ion is present, the pH at the equivalence point is found from its base ionization. The acetate concentration is used in an ICE setup, and x is assumed to be much less than 0.0500. The pH at this point is significantly greater than 7, which is expected for a weak acid titrated with a strong base.

At 12.50 mL of NaOH, the titration is at the half-equivalence point. This is one-half of the stoichiometric amount of titrant, so one-half of the acetic acid has been neutralized. Equal amounts of acetic acid and acetate are present, and the Henderson-Hasselbalch equation is a convenient way to find the pH. At the half-equivalence point, pH equals pKa.

At 37.50 mL of NaOH, there is a stoichiometric excess of titrant. The reaction mixture contains acetate ion from the titration product and extra strong base. In this case, the pH is determined mainly by the amount of excess base.

pH at Key Points in a Weak Acid Titration

ph-at-key-points-in-a-weak-acid-titration

common ion effect

Common Ion Effect on Solubility

The common ion effect reduces the solubility of an ionic compound in a solution that already contains one of its ions. In aqueous solutions, this means less of the solid dissolves than it would in pure water. The effect follows the law of mass action and can be explained with Le Châtelier’s principle. Silver iodide shows this equilibrium clearly. When silver(I) ions or iodide ions are added, the dissolution equilibrium shifts left. More AgI precipitates, and the concentrations of dissolved Ag+...

buffers

Buffer Solutions and pH Stability

Buffer solutions are mixtures that help keep pH steady. A buffer contains an appreciable amount of a weak conjugate acid-base pair. It resists a change in pH when small amounts of a strong acid or a strong base are added. One common buffer uses a weak acid and its salt. Acetic acid and sodium acetate form this type of system, written as CH3COOH(aq) + CH3COONa(aq). Another buffer uses a weak base and its salt. A solution of ammonia and ammonium chloride, NH3(aq) + NH4Cl(aq), is an example. The...

calculating ph changes in a buffer solution

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Buffer pH After Acid or Base Addition

A buffer solution can resist sudden pH changes when a strong acid or strong base is added. It does not stop the pH from changing completely. The shift is usually small, as long as the addition stays within the buffer’s capacity. To find the new pH, first determine how the added acid or base changes the amounts of the buffer components. A buffer contains a weak acid and its conjugate base, or the reverse pair. These amounts are found with stoichiometric calculations, which track how much of...

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Buffer Capacity and pH Stability

Buffer solutions help keep pH fairly constant, but they do not work forever. Their resistance to pH change depends on having enough of a weak acid and its conjugate base, or a weak base and its conjugate acid, in the mixture. When too much strong acid or strong base is added, one part of the buffer pair is used up and the buffer action becomes weaker. Buffer capacity describes how much acid or base can be added to a fixed volume of buffer before the pH changes noticeably, usually by about one...

titration calculations: strong acid - strong base

titration-calculations-strong-acid-strong-base

pH at Key Points in Acid-Base Titration

pH at key points in a strong acid and strong base titration can be calculated from the amounts of acid and base present. The example uses 25.00 mL of 0.100 M HCl, a strong acid, and 0.100 M NaOH, a strong base. The pH changes as base is added, and each stage follows a different calculation. At 0 mL of titrant, the pH comes from the ionization of HCl. Because HCl is a strong acid, its ionization is complete. The hydronium ion molarity is 0.100 M, and the pH is found from that value. At 12.50...

titration calculations: weak acid - strong base

pH at key points in a weak acid titration can be calculated for an acetic acid solution as sodium hydroxide is added. The example uses 25.00 mL of 0.100 M CH3CO2H titrated with 0.100 M NaOH. The reaction is shown as the weak acid reacts with the strong base. The initial pH is found from the acetic acid solution using the usual ICE approach. ICE means initial, change, and equilibrium, and it is a common way to set up equilibrium problems. The solution pH is calculated before any titrant is...

indicators

Acid-Base Color Changes

Acid-base indicators show color changes that help identify the pH of a solution. These are often weak organic acids or weak organic bases, and they respond to changes in hydronium ion concentration in dilute aqueous solution. Phenolphthalein is one example. It is colorless when the hydronium ion concentration is greater than 5.0 × 10^-9 M, which means the pH is below 8.3. In more basic solutions, where the hydronium ion concentration is lower, it turns red or pink. Methyl orange shows how an...

titration of a polyprotic acid

Polyprotic Acid Equivalence Points

Polyprotic acids have more than one ionizable hydrogen, so they lose protons in steps during titration. When the acid dissociation constants for those protons are far enough apart, the titration curve shows a separate equivalence point for each hydrogen that can ionize. Diprotic acids have two ionizable hydrogens and produce two equivalence points. Triprotic acids have three ionizable hydrogens and produce three equivalence points. Carbonic acid, H2CO3, is a weak diprotic acid. Carbonic acid...

solubility equilibria

Predicting Precipitation with Ksp

Solubility equilibria explain how a dissolved ionic compound and its solid form can exist in balance. In a saturated solution, the solute dissolves and the ions precipitate at equal rates. These ideas matter in real settings such as tooth decay and water purification, where compound solubility affects the outcome. A substance with finite solubility can form a saturated solution when more solute is added than the solvent can dissolve. The result is a heterogeneous mixture of the saturated...

factors affecting solubility

Common Ion Effects on Solubility

The common ion effect lowers the solubility of an ionic compound in water when the solution already contains one of the ions made by that compound. It follows the law of mass action and can be explained with Le Châtelier’s principle. When a common ion is added, the dissolution equilibrium shifts toward the solid, so less of the salt stays dissolved. Silver iodide shows this effect clearly. If silver ions or iodide ions are added to a solution of AgI, the equilibrium shifts left and more AgI...

formation of complex ions

Ligands and Complex Ion Stability

Complex ions form when a central atom, often a transition metal cation, binds to ligands. Ligands are ions or molecules around the metal ion. They can be neutral molecules such as H2O or NH3, or ions such as CN− or OH−. In many cases, the ligands act as Lewis bases by donating a pair of electrons to the central atom. These reactions are part of coordination chemistry, which studies coordination complexes. When a metal ion reacts with one or more ligands to form a complex, the equilibrium...

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Solubility Limits and Selective Precipitation

Solubility limits and selective precipitation explain when ions form a solid in water. The key idea is the balance between an insoluble compound and its dissolved ions. In aqueous solutions that contain calcium ions and carbonate ions, this equilibrium can exist even if the solution was not made by saturating water with calcium carbonate. When two soluble salts are mixed, such as sodium carbonate and calcium nitrate, the ion concentrations determine whether a precipitate forms. If the reaction...

qualitative analysis

Cation Identification by Precipitation Tests

Cation identification by precipitation tests uses selective reactions to find metal ions in a mixture. In qualitative analysis, different reagents are added step by step. Each reaction can produce a characteristic precipitate for a specific group of cations. Other steps, such as changing pH, heating the mixture to dissolve a precipitate again, or adding reagents that form complex ions, help separate ions within the same group. Group IV cations such as Ba2+, Ca2+, and Mg2+ are identified...

henderson-hasselbalch equation

Buffer pH with the Henderson-Hasselbalch Equation

The Henderson-Hasselbalch equation helps relate buffer pH to the weak acid in the solution. It comes from the ionization-constant expression for a weak acid. By rearranging that expression to solve for hydronium ion concentration, [H3O+], and then taking the negative logarithm of both sides, the equation can be written in terms of pH. In this form, pKa is defined as the negative logarithm of the weak acid ionization constant, or pKa = −log Ka. The equation shows the connection between pH, pKa,...

acid-base titration curves

Tracking pH During Acid-Base Titration

Acid-base titration uses pH changes to track how a solution responds as titrant is added. A titration curve is a graph of a solution property versus the amount of added titrant. In acid-base titrations, pH is the main property to follow because it changes in a predictable way with the solution makeup and helps show the endpoint. This pattern can be seen with a strong acid and strong base, a strong acid and weak base, or a strong base and weak acid. For example, 25.00 mL of 0.100 M HCl titrated...

key terms and concepts

Follow how pH changes during a weak acid titration with strong base, including the initial solution, half-equivalence point, equivalence point, and excess base.

pH at Key Points in a Weak Acid Titration | JoVE K12

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Homogeneous Equilibria for Gaseous Reactions

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Relative Strengths of Conjugate Acid-Base Pairs

Br&#248;nsted-Lowry acid-base chemistry is the transfer of protons; thus, logic suggests a relation between the relative strengths of conjugate acid-base ...

Calculating Equilibrium Concentrations

Being able to calculate equilibrium concentrations is essential to many areas of science and technology&#8212;for example, in the formulation and dosing ...

Strong Acid and Base Solutions

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The Small x Assumption

If a reaction has a small equilibrium constant, the equilibrium position favors the reactants. In such reactions, a negligible change in concentration may ...

Weak Acid Solutions

Few compounds act as strong acids. A far greater number of compounds behave as weak acids and only partially react with water, leaving a large majority of ...

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Le Chatelier's Principle: Changing Concentration

A system at equilibrium is in a state of dynamic balance, with forward and reverse reactions taking place at equal rates. If an equilibrium system is ...

Weak Base Solutions

Some compounds produce hydroxide ions when dissolved by chemically reacting with water molecules. In all cases, these compounds react only partially and ...

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Le Chatelier's Principle: Changing Volume (Pressure)

For gas-phase equilibria, changes in the concentrations of reactants and products can occur with altered volume and pressure. The partial pressure, P, of ...

Mixtures of Acids

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Le Chatelier's Principle: Changing Temperature

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Salts with Acidic Ions
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Bronsted-Lowry Acids and Bases

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Determining the pH of Salt Solutions

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acidbase-strengths-and-dissociation-constants

Acid/Base Strengths and Dissociation Constants

The relative strength of an acid or base is the extent to which it ionizes when dissolved in water. If the ionization reaction is essentially complete, ...

Polyprotic Acids

Acids are classified by the number of protons per molecule that they can give up in a reaction. Acids such as HCl, HNO3, and HCN that contain one ...

Water: A Bronsted-Lowry Acid and Base

The reaction between a Br&#248;nsted-Lowry acid and water is called acid ionization. For example, when hydrogen fluoride dissolves in water and ionizes, ...

Chemical reactions
• Types of reactions
• Kinetics
• Energy
• Equilibrium
• Acids/bases

Content elaboration: In the Physical Science course, coefficients were used to balance simple equations. Other representations, including Lewis structures and three-dimensional models, were also used and manipulated to demonstrate the conservation of matter in chemical reactions. In this course, more complex reactions will be studied, classified and represented with balanced chemical equations and three-dimensional models. Classifying reactions into types can be a helpful organizational tool for recognizing patterns of what may happen when two substances are mixed. Teachers should be aware that the common reaction classifications that are often used in high school chemistry courses may lead to misconceptions because they are not based on the actual chemistry, but on surface features that can be similar from one system to another (e.g., exchanging partners), even though the underlying chemistry is not the same. However, these classifications may be useful in making predictions about what happens when two substances are mixed. Some general types of chemical reactions are oxidation/reduction, synthesis, decomposition, single replacement, double replacement (including precipitation reactions and some acid-base neutralizations) and combustion reactions. Some reactions can fit into more than one category. For example, a single replacement reaction can also be classified as an oxidation/reduction reaction. Identification of reactions involving oxidation and reduction as well as indicating what substance is being oxidized and what is being reduced are appropriate in this course. However, balancing complex oxidation/reduction reactions is reserved for more advanced study. Organic molecules release energy when undergoing combustion reactions and are used to meet the energy needs of society (e.g., oil, gasoline, natural gas) and to provide the energy needs of biological organisms (e.g., cellular respiration). When a reaction between two ionic compounds in aqueous solution results in the formation of a precipitate or molecular compound, the reaction often occurs because the new ionic or covalent bonds are stronger than the original ion-dipole interactions of the ions in solution. Laboratory experiences (3-D or virtual) with different types of chemical reactions should be provided. Reactions occur when reacting particles collide in an appropriate orientation and with sufficient energy. The rate of a chemical reaction is the change in the amount of the reactants or products in a specific period of time. Increasing the probability or effectiveness of the collisions between the particles increases the rate of the reaction. Therefore, changing the concentration of the reactants, changing the temperature or the pressure of gaseous reactants, or using a catalyst, can change the reaction rate. Likewise, the collision theory can be applied to dissolving solids in a liquid solvent and can be used to explain why reactions are more likely to occur between reactants in the aqueous or gaseous state than between solids. The rate at which a substance dissolves should not be confused with the amount of solute that can dissolve in a given amount of solvent (solubility). Mathematical treatment of reaction rates is reserved for more advanced study. Computer simulations can help visualize reactions from the perspective of the kinetic-molecular theory. In middle school, the differences between potential and kinetic energy and the particle nature of thermal energy were introduced. For chemical systems, potential energy is in the form of chemical energy and kinetic energy is in the form of thermal energy. The total amount of chemical energy and/or thermal energy in a system is impossible to measure. However, the energy change of a system can be calculated from measurements (mass and change in temperature) from calorimetry experiments in the laboratory. Conservation of energy is an important component of calorimetry equations. Thermal energy is the energy of a system due to the movement of its particles. The thermal energy of an object depends upon the temperature and chemical composition. Some materials require little energy to change their temperature and other materials require a great deal to change their temperature by the same amount. Specific heat is a measure of how much energy is needed to change the temperature of a specific mass of material a specific amount. Specific heat values can be used to calculate the thermal energy change, the temperature (initial, final or change in) or mass of a material in calorimetry. Water has a particularly high specific heat capacity, which is important in regulating Earth's temperature. As studied in middle school, chemical energy is the potential energy associated with chemical systems. Chemical reactions involve valence electrons forming bonds to yield more stable products with lower energies. Energy is required to break interactions and bonds between the reactant atoms and energy is released when an interaction or bond is formed between the atoms in the products. Molecules with weak bonds (e.g., ATP) are less stable and tend to react to produce more stable products, releasing energy in the process. Generally, energy is transferred out of the system (exothermic) when the products have stronger bonds than the reactants and is transferred into the system (endothermic) when the reactants have stronger bonds than the products. Predictions of the energy requirements (endothermic or exothermic) of a reaction can be made given a table of bond energies. Graphic representations can be drawn and interpreted to represent the energy changes during a reaction. The role of energy in determining the spontaneity of chemical reactions is dealt with conceptually in this course. Entropy and its influence on the spontaneity of reactions are reserved for more advanced study. All reactions are reversible to a degree and many reactions do not proceed completely toward products but appear to stop progressing before the reactants are all used up. At this point, the amounts of the reactants and the products appear to be constant and the reaction can be said to have reached dynamic equilibrium. Dynamic equilibrium means the rate of the reverse reaction is equal to the rate of the forward reaction so there is no apparent change in the reaction. If a chemical system at equilibrium is disturbed by a change in the conditions of the system (e.g., increase or decrease in the temperature, pressure on gaseous equilibrium systems, concentration of a reactant or product), then the equilibrium system will respond by shifting to a new equilibrium state, reducing the effect of the change (Le Chatelier's Principle). If products are removed as they are formed during a reaction, then the equilibrium position of the system is forced to shift to favor the products. In this way, an otherwise unfavorable reaction can be made to occur. Mathematical treatment of equilibrium reactions is reserved for advanced study. Computer simulations can help visualize the progression of a reaction to dynamic equilibrium and the continuation of both the forward and reverse reactions after equilibrium has been attained. Properties of acids and bases and the ranges of the pH scale were introduced in Physical Science. In this course, the structural features of molecules are explored to further understand acids and bases. Acids often result when hydrogen is covalently bonded to an electronegative element and is easily dissociated from the rest of the molecule to bind with water to form a hydronium ion (H3O+). The acidity of an aqueous solution can be expressed as pH, where pH can be calculated from the concentration of the hydronium ion. Bases are likely to dissociate in water to form a hydroxide ion. Acids can react with bases to form a salt and water. Such neutralization reactions can be studied quantitatively by performing titration experiments.

pH at Key Points in a Weak Acid Titration

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