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Assertion : Rate of hydrolysis of methyl...

Assertion : Rate of hydrolysis of methyl chloride to methanol is higher in DMF than in water.
Reason : Hydrolysis of methyl chloride follows second order kinetics.

A

If both assertion and reason are true and reason is the correct explanation of assertion

B

If both assertion and reason are true but reason is not the correct explanation of assertion

C

If assertion is true but reason is false

D

If both assertion and reason are false

Text Solution

AI Generated Solution

The correct Answer is:
To solve the question, we will analyze both the assertion and the reason provided. ### Step 1: Understand the Assertion The assertion states that "the rate of hydrolysis of methyl chloride to methanol is higher in DMF than in water." - Methyl chloride (CH3Cl) undergoes hydrolysis in a nucleophilic substitution reaction (SN2 mechanism) where the nucleophile (water or hydroxide ion) attacks the carbon atom, leading to the formation of methanol (CH3OH) and chloride ion (Cl⁻). - DMF (Dimethylformamide) is a polar aprotic solvent, while water is a polar protic solvent. ### Step 2: Analyze the Role of Solvents In SN2 reactions, the choice of solvent significantly affects the reaction rate: - Polar protic solvents (like water) can stabilize the nucleophile and the transition state through hydrogen bonding, which can hinder the reaction. - Polar aprotic solvents (like DMF) do not have hydrogen bonding capabilities that stabilize the nucleophile, allowing it to remain more reactive. ### Conclusion for Assertion Since DMF is a polar aprotic solvent, it enhances the rate of hydrolysis of methyl chloride compared to water. Thus, the assertion is **true**. ### Step 3: Understand the Reason The reason states that "hydrolysis of methyl chloride follows second order kinetics." - In an SN2 reaction, the rate of reaction depends on the concentration of both the substrate (methyl chloride) and the nucleophile (water or hydroxide ion). - This means the reaction is second order overall because the rate law can be expressed as Rate = k[CH3Cl][Nucleophile]. ### Conclusion for Reason Since the hydrolysis of methyl chloride indeed follows second order kinetics, the reason is also **true**. ### Final Conclusion Both the assertion and the reason are true, and the reason correctly explains the assertion. ### Answer Both the assertion and reason are true, and the reason is the correct explanation of the assertion. ---

To solve the question, we will analyze both the assertion and the reason provided. ### Step 1: Understand the Assertion The assertion states that "the rate of hydrolysis of methyl chloride to methanol is higher in DMF than in water." - Methyl chloride (CH3Cl) undergoes hydrolysis in a nucleophilic substitution reaction (SN2 mechanism) where the nucleophile (water or hydroxide ion) attacks the carbon atom, leading to the formation of methanol (CH3OH) and chloride ion (Cl⁻). - DMF (Dimethylformamide) is a polar aprotic solvent, while water is a polar protic solvent. ...
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