Shown below is the structure of methyl acetate with three different $\alpha, \beta$ and $\gamma$ carbon - oxygen bonds.

The correct order of bond lengths of these bonds is :
Given below are two statements :
Statement I : On the basis of inductive effect, the order of stability of alkyl carbanions is $\mathrm{CH}_3{ }^{-}>\mathrm{CH}_3-\mathrm{CH}_2{ }^{-}>\left(\mathrm{CH}_3\right)_2 \mathrm{CH}^{-}>\left(\mathrm{CH}_3\right)_3 \mathrm{C}^{-}$.
Statement II : Allyl and benzyl carbanions are more stabilised by inductive effect and not by resonance effect.
In the light of the above statements, choose the correct answer from the options given below :
$$ \text { Match the LIST-I with LIST-II } $$
| List-I Reaction |
List-I Mechanism |
||
|---|---|---|---|
| A. | Williamson Synthesis | I. | Electrophilic addition |
| B. | Friedel Craft Reaction | II. | Free radical substitution |
| C. | Bromination of vinyl benzene | III. | Nucleophilic substitution |
| D. | Chlorination of toluene in light | IV. | Electrophilic substitution |
Choose the correct answer from the options given below:
$$ \text { Consider the following molecules/species : } $$
$$ \text { The correct order of carbon-oxygen double bond length is : } $$
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