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Quaternary ammonium salt is formed
  • a)
    by serial nucleophilic substitution of the product
  • b)
    By treating an alkyl or benzyl halide with ammonia
  • c)
    By nucleophilic substitution reaction
  • d)
    all of these
Correct answer is option 'D'. Can you explain this answer?
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Quaternary ammonium salts are formed by a series of nucleophilic substitution reactions, which involve the substitution of a nucleophile for a leaving group. The correct answer is option 'D' because all of the given options are valid methods for the formation of quaternary ammonium salts. Let's discuss each option in detail:

a) Serial nucleophilic substitution of the product:
This option refers to a stepwise process in which a nucleophile substitutes a leaving group in a reaction, producing an intermediate product. This intermediate product then undergoes further nucleophilic substitution reactions until the desired quaternary ammonium salt is obtained.

b) Treating an alkyl or benzyl halide with ammonia:
Alkyl or benzyl halides can react with ammonia (NH3) to form quaternary ammonium salts. In this reaction, the halide group is replaced by an ammonium group, resulting in the formation of a quaternary ammonium salt.

c) Nucleophilic substitution reaction:
Nucleophilic substitution reactions involve the substitution of a nucleophile for a leaving group. In the case of quaternary ammonium salts, a nucleophile replaces a leaving group attached to a quaternary ammonium ion, resulting in the formation of a new quaternary ammonium salt.

Therefore, all of the given options are valid methods for the formation of quaternary ammonium salts. These salts are widely used in various applications, including as surfactants, disinfectants, and catalysts.
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Read the passage given below and answer the following questions:Reductive alkylation is the term applied to the process of introducing alkyl groups into ammonia or a primary or secondary amine by means of an aldehyde or ketone in the presence of a reducing agent. The present discussion is limited to those reductive alkylations in which the reducing agent is hydrogen and a catalyst or "nascent" hydrogen, usually from a metalacid combination; most of these reductive alkylations have been carried out with hydrogen and a catalyst. The principal variation excluded is that in which the reducing agent is formic acid or one of its derivatives; this modification is known as the Leuckart reaction. The process of reductive alkylation of ammonia consists in the addition of ammonia to a carbonyl compound and reduction of the addition compound or its dehydration product. The reaction usually is carried out in ethanol solution when the reduction is to be effected catalytically:Since the primary amine is formed in the presence of the aldehyde it may react in the same way as ammonia, yielding an additional compound, a Schiff's base (RCH= NCH2R) and finally, a secondary amine. Similarly, the primary amine may react with the imine, forming an addition product which also is reduced to a secondary amine Finally, the secondary amine may react with either the aldehyde or the imine to give products which are reduced to tertiary amines.Similar reactions may occur when the carbonyl compound employed is a ketone.Q. The reaction of ammonia and its derivatives with aldehydes is called

Quaternary ammonium salt is formeda)by serial nucleophilic substitution of the productb)By treating an alkyl or benzyl halide with ammoniac)By nucleophilic substitution reactiond)all of theseCorrect answer is option 'D'. Can you explain this answer?
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