Home
Class 12
CHEMISTRY
Statement-1: Acid catalysed dehydration ...

Statement-1: Acid catalysed dehydration of t-butanol is faster than n-butanol.
Statement-2: The order of stability of carbocation is `3^(@)gt2^(@)gt1^(@)`.

A

Statement-1 is True, Statement-2 is True, Statement-2 is a correct explanation for statement-1

B

statement-1 is true, statement-2 is true, statement-2 is NOT a correct explanation for statement-1

C

statement-1 is true, statement-2 is false

D

statement-1 is false, statement-2 is true

Text Solution

AI Generated Solution

The correct Answer is:
To analyze the statements provided in the question, we will break down the reasoning step by step. ### Step 1: Understanding the Statements - **Statement 1**: Acid-catalyzed dehydration of t-butanol is faster than n-butanol. - **Statement 2**: The order of stability of carbocations is 3° > 2° > 1°. ### Step 2: Analyzing Statement 1 - Tertiary butanol (t-butanol) is represented as (CH₃)₃COH, while n-butanol is represented as CH₃CH₂CH₂OH. - When these alcohols undergo dehydration in the presence of an acid (like concentrated sulfuric acid), they form carbocations. - The reaction mechanism involves protonation of the alcohol, followed by loss of water to form a carbocation. ### Step 3: Carbocation Formation - For t-butanol: - Protonation leads to the formation of a tertiary carbocation: (CH₃)₃C⁺. - For n-butanol: - Protonation leads to the formation of a primary carbocation: CH₃CH₂CH₂⁺. ### Step 4: Stability of Carbocations - The stability of carbocations follows the order: tertiary (3°) > secondary (2°) > primary (1°). - Tertiary carbocations are stabilized by the inductive effect of the surrounding alkyl groups, making them more stable than primary carbocations. ### Step 5: Conclusion for Statement 1 - Since t-butanol forms a more stable tertiary carbocation compared to the primary carbocation formed from n-butanol, the dehydration of t-butanol is indeed faster than that of n-butanol. - Therefore, **Statement 1 is true**. ### Step 6: Conclusion for Statement 2 - The order of stability of carbocations (3° > 2° > 1°) is a well-established principle in organic chemistry. - Therefore, **Statement 2 is also true**. ### Step 7: Relationship Between the Statements - Statement 2 explains why Statement 1 is true: the faster dehydration of t-butanol is due to the stability of the tertiary carbocation formed during the reaction. - Thus, Statement 2 is a correct explanation for Statement 1. ### Final Conclusion Both statements are true, and Statement 2 correctly explains Statement 1. Therefore, the correct option is that both statements are true, and Statement 2 is a correct explanation for Statement 1.
Promotional Banner

Similar Questions

Explore conceptually related problems

Acid catalysed dehydration of t-butanol is faster than that of n-butanol because

The reactivity order of alkyl halide is 3^(@) gt 2^(@) gt 1^(@) in

The reactivity of carbanions follows the order 3^@ gt 2^@ gt 1^@ .

Statement - 1 POCl_(3) can be used to dehydrate alcohols Statement -2 This reaction proceeds by formation of carbocation in 1^(st) step

Statement-1: Bridge head carbocation is less stable than Bridge head carbanion. and Statement-2: C atom in carbocation is sp^(2) generally hybridized.

Statement-1: Keto form is less stable than enol form and Statement-2: Enol form is stabilized by aromaticity.

The major product of acid catalysed dehydration of 2-methylcyclohexanol and butan-1-ol are respectively

Statement -1 : S_(N)2 reaction of CH_(3) -Br faster in DMSO than in H_(2)O Statement -2 : DMSO has greater capability to solvate nucleophile

Statement-1- 1 Phenol is more acidic than water Statement-2 Phenoxide ion is resonance stabilized.

Statement -1 : Rate of S_(N)1 reaction is faster than that of S_(N)2 reaction Statement -2 : S_(N)2 reaction is favoured by polar aprotic solvent Statement -3 : S_(N)1 reaction involves racemization