Problem 38
Question
Carbylamine test is performed in alcoholic \(\mathrm{KOH}\) by heating a mixture of :(a) chloroform and silver powder (b) trihalogenatedmethane and a primary amine (c) an alkyl halide and a primary amine (d) an alkyl cyanide and a primary amine
Step-by-Step Solution
Verified Answer
The carbylamine test is performed with (b) trihalogenatedmethane and a primary amine.
1Step 1: Understanding Carbylamine Reaction
The Carbylamine reaction is used to identify primary amines. It involves heating a mixture of a primary amine, chloroform, and alcoholic potassium hydroxide (KOH) to produce an isocyanide, which has a characteristic unpleasant odor.
2Step 2: Identifying Key Reactants
The key reactants in the Carbylamine test are a primary amine, chloroform (a trihalogenated methane), and an alcoholic KOH solution. We need to identify which option provides these reactants.
3Step 3: Analyzing Each Option
- (a) Chloroform and silver powder: Does not include a primary amine.
- (b) Trihalogenatedmethane and a primary amine: Takes into account chloroform as trihalogenated methane and a primary amine, fulfilling the Carbylamine reaction requirements.
- (c) An alkyl halide and a primary amine: Lacks chloroform/trihalogenated methane.
- (d) An alkyl cyanide and a primary amine: Also lacks chloroform/trihalogenated methane.
4Step 4: Selecting the Correct Option
Based on the conditions of the Carbylamine test, option (b) provides both trihalogenatedmethane (chloroform) and a primary amine necessary for the reaction. Thus, the correct answer is (b).
Key Concepts
Primary Amine IdentificationIsocyanide FormationOrganic Chemistry Reactions
Primary Amine Identification
Identifying a primary amine is crucial in various chemical processes, including the Carbylamine test. A primary amine is an organic compound containing a nitrogen atom bonded to one carbon atom (other than any carbonyl carbon) and two hydrogen atoms. It is essential in the formation of isocyanides during the Carbylamine test.
In practical terms, primary amines are tested by their ability to undergo specific reactions, such as the Carbylamine test, where their presence leads to the formation of an isocyanide. This reaction is sensitive to primary amines and does not occur with secondary or tertiary amines, making it a reliable identification method.
In practical terms, primary amines are tested by their ability to undergo specific reactions, such as the Carbylamine test, where their presence leads to the formation of an isocyanide. This reaction is sensitive to primary amines and does not occur with secondary or tertiary amines, making it a reliable identification method.
- Primary amine structure: R-NH2, where R is an alkyl or aryl group.
- Reactivity: Primary amines readily react under certain conditions, making them easy to test for.
Isocyanide Formation
Isocyanide formation is a key indicator in the Carbylamine test. It provides a distinctive, pungent odor, helping chemists confirm the presence of primary amines. The process involves the conversion of primary amines, chloroform, and alcoholic potassium hydroxide (KOH) into isocyanides.
The isocyanide reaction proceeds as follows:
The isocyanide reaction proceeds as follows:
- The primary amine reacts with chloroform (CHCl3) in the presence of strong base, alcoholic KOH.
- Upon heating, a complex series of reactions ensue, forming the isocyanide (R-NC) and releasing water and potassium chloride.
Organic Chemistry Reactions
Organic chemistry reactions, such as the Carbylamine reaction, are pivotal in transforming compounds and identifying various molecular structures. This area of chemistry focuses on the behavior of carbon-containing compounds and their interactions with other elements like hydrogen, oxygen, and nitrogen.
In the context of the Carbylamine reaction, understanding the basic principles of organic reactions helps in grasping how primary amines are converted into isocyanides. Reactions in organic chemistry often involve:
In the context of the Carbylamine reaction, understanding the basic principles of organic reactions helps in grasping how primary amines are converted into isocyanides. Reactions in organic chemistry often involve:
- Formation or breaking of chemical bonds between carbon and other elements.
- Presence of catalysts or conditions like temperature changes that facilitate reaction progress.
Other exercises in this chapter
Problem 36
In the reaction \(p\)-chlorotoluene with \(\mathrm{KNH}_{2}\) in liq. \(\mathrm{NH}_{3}\),the major product is:(a) \(o\)-toluidine (b) \(m\)-toluidine (c) \(p\)
View solution Problem 37
Amongst the following, the most basic compound is :(a) Benzylamine (b) Aniline (c) Acetanilide (d) \(p\)-Nitroaniline
View solution Problem 39
Acetamide is treated separately with the following reagents. Which one of these would give methylamine?(a) \(\mathrm{PCl}_{5}\) (b) \(\mathrm{NaOH}+\mathrm{Br}_
View solution Problem 40
The compound which on reaction with aqueous nitrous acid at low temperature produces an oily nitrosoamine is(a) methylamine (b) ethylamine (c) diethylamine (d)
View solution