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प्रश्न
Allyl chloride is hydrolysed more readily than n-propyl chloride. Why?
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उत्तर
Allyl chloride shows high reactivity because the carbocation formed by hydrolysis is stabilised by resonance while no such stabilisation of carbocation exists in the case of n-propyl chloride.
संबंधित प्रश्न
Write the final product(s) in each of the following reactions:
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Give reasons:
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Write chemical equation in support of your answer.
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Cl and 
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Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.
| (a) |  |
| (b) |  |
| (c) |  |
Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.
| (a) |  |
| (b) |  |
| (c) |  |
Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.
| (a) |  |
| (b) |  |
| (c) |  |
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| (a) |  |
| (b) |  |
| (c) |  |
Haloarenes are less reactive than haloalkanes and haloalkenes. Explain.
\[\ce{C6H12O6 ->[(Zymase)] A ->[NaOH][\Delta] B + CHI3}\]
The number of carbon atoms present in the product B is:
Assertion: Chlorobenzene is resistant to nucleophilic substitution reaction at room temperature.
Reason (R): C–Cl bond gets weaker due, to resonance.
Why haloarenes are not reactive towards nucleophilic substitution reaction? Give two reactions.
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\[\ce{CH3CHO \underset{ii) H2O+}{\overset{i) LiAlH4}{->}} [A] \underset{\triangle}{\overset{H2SO4}{->}} [B]}\]
