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In the diazotisation of anline with sodi...

In the diazotisation of anline with sodium nitrite and hydrochloride acid, an excess of hydrochloric acid is used primarily to

A

Suppress the concentration of free aniline for coupling

B

Suppress hydrolysis of phenol

C

Ensure a stoichiometric amount of nitrous acid

D

Neutralize the base liberated

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The correct Answer is:
To answer the question regarding the use of excess hydrochloric acid in the diazotisation of aniline with sodium nitrite, we can break down the process step by step. ### Step-by-Step Solution: 1. **Understanding Diazotisation**: - Diazotisation is a chemical reaction that involves converting an amine (in this case, aniline) into a diazonium salt. Aniline (C6H5NH2) reacts with sodium nitrite (NaNO2) in the presence of hydrochloric acid (HCl) to form benzene diazonium chloride (C6H5N2Cl). 2. **Reaction Components**: - The main components of the reaction are: - Aniline (C6H5NH2) - Sodium nitrite (NaNO2) - Hydrochloric acid (HCl) 3. **Role of Hydrochloric Acid**: - Hydrochloric acid serves multiple purposes in this reaction. It provides the acidic medium necessary for the formation of the diazonium ion from the aniline. 4. **Excess Hydrochloric Acid**: - An excess of hydrochloric acid is used to suppress the concentration of free aniline in the solution. This is crucial because free aniline can lead to unwanted side reactions, particularly coupling reactions, where the diazonium salt could react with the aniline itself, leading to the formation of azo compounds. 5. **Preventing Coupling Reactions**: - If the concentration of free aniline is high, the diazonium salt (C6H5N2+) can couple with the aniline, resulting in undesired products. By using excess HCl, we ensure that the aniline is protonated (forming anilinium ions, C6H5NH3+), which reduces the availability of free aniline for coupling reactions. 6. **Conclusion**: - Therefore, the primary reason for using excess hydrochloric acid in the diazotisation of aniline is to suppress the concentration of free aniline, thus preventing coupling reactions and ensuring the successful formation of the diazonium salt. ### Final Answer: The excess hydrochloric acid is used primarily to suppress the concentration of free aniline for coupling.

To answer the question regarding the use of excess hydrochloric acid in the diazotisation of aniline with sodium nitrite, we can break down the process step by step. ### Step-by-Step Solution: 1. **Understanding Diazotisation**: - Diazotisation is a chemical reaction that involves converting an amine (in this case, aniline) into a diazonium salt. Aniline (C6H5NH2) reacts with sodium nitrite (NaNO2) in the presence of hydrochloric acid (HCl) to form benzene diazonium chloride (C6H5N2Cl). 2. **Reaction Components**: ...
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RESONANCE ENGLISH-NITROGEN CONTAINING COMPOUNDS-ORGANIC CHEMISTRY(Nitrogen containing Compounds)
  1. Which of the following is capable of forming a zwitter ion ?

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  2. The uncertainties in position and the velocity of a particle are 10^(-...

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  3. In the diazotisation of anline with sodium nitrite and hydrochloride a...

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  4. Starting from propanoic acid, the following reaction were carried acid...

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  5. In the reaction, C(6)H(5)NH(2)underset(0-5^(@)C)overset(NaNO(2)+HCl)...

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  6. In the given reaction product P is :

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  7. P ( major product ), P is

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  8. Identify A,C(6)H(11)N, for which the given information is availabel . ...

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  9. An optically inactive amine (A) is methylated with excess of CH(3)I an...

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  10. The product P formed in the given reaction sequence is .

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  11. Identify the correct statement.

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  12. Which statement is incorrect.

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  13. What will be the major product when 2-Aminopropane is treated with nit...

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  14. Which of the following product (s) will be obtained when isopropylamin...

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  15. Which of the following compounds will give N(2)(g) on treatment with H...

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  16. Compound (x)(m.f=C(7)H(8)N), on reaction with NaNO(2) and conc. HCl at...

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  17. Pyridine is less basic than triethylamine because

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  18. The reagents are

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  19. Arrange following Amines for rate of reaction with CHCl(3)+KOH ?

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  20. Which of the following is correct order of basic strength for the give...

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