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In esterfication reaction rate for diffe...

In esterfication reaction rate for different alcohols

A

`3^(@) gt 1^(@) gt 2^(@)`

B

`2 ^(@) gt 3^(@) gt 1^(@)`

C

`1 ^(@) gt 2^(@) gt 3^(@)`

D

none of these

Text Solution

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The correct Answer is:
To analyze the rate of esterification reactions for different alcohols, we can follow these steps: ### Step 1: Understand the Esterification Reaction Esterification is a reaction between a carboxylic acid (RCOOH) and an alcohol (ROH) in the presence of an acid catalyst (H+). The general reaction can be represented as: \[ \text{RCOOH} + \text{ROH} \rightarrow \text{RCOOR} + \text{H}_2\text{O} \] ### Step 2: Mechanism of the Reaction 1. **Protonation of Alcohol**: The acid protonates the oxygen of the alcohol, increasing its electrophilicity. 2. **Nucleophilic Attack**: The protonated alcohol (ROH2+) attacks the carbonyl carbon of the carboxylic acid, forming a tetrahedral intermediate. 3. **Formation of Ester**: The tetrahedral intermediate collapses, leading to the formation of the ester and the release of water. ### Step 3: Analyze the Role of Alcohol Structure The structure of the alcohol affects the stability of the transition state during the reaction: - **1° Alcohols**: Have less steric hindrance, leading to a more stable transition state and a faster reaction rate. - **2° Alcohols**: Have moderate steric hindrance, resulting in a slower reaction rate compared to 1° alcohols. - **3° Alcohols**: Have significant steric hindrance, making the transition state unstable and resulting in the slowest reaction rate. ### Step 4: Rate Order for Different Alcohols Based on the stability of the transition states: - **1° Alcohols**: Fastest reaction rate (least steric hindrance) - **2° Alcohols**: Moderate reaction rate - **3° Alcohols**: Slowest reaction rate (most steric hindrance) ### Conclusion The order of the reaction rate for esterification with different alcohols is: \[ \text{1° Alcohol} > \text{2° Alcohol} > \text{3° Alcohol} \] ### Final Answer The rate of esterification is highest for 1° alcohols, followed by 2° alcohols, and lowest for 3° alcohols. ---

To analyze the rate of esterification reactions for different alcohols, we can follow these steps: ### Step 1: Understand the Esterification Reaction Esterification is a reaction between a carboxylic acid (RCOOH) and an alcohol (ROH) in the presence of an acid catalyst (H+). The general reaction can be represented as: \[ \text{RCOOH} + \text{ROH} \rightarrow \text{RCOOR} + \text{H}_2\text{O} \] ### Step 2: Mechanism of the Reaction 1. **Protonation of Alcohol**: The acid protonates the oxygen of the alcohol, increasing its electrophilicity. ...
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