Allyl chloride is hydrolysed more readily than n-propyl chloride. Why?
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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.
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Write the structure of the major organic product in each of the following reaction:
$\text{CH}_3\text{CH}_2\text{CH}_2\text{OH}+\text{SOCl}_2\xrightarrow{}$
Name the following halides according to $\text{IUPAC}$ system and classify them as alkyl, allyl, benzyl $($primary, secondary, tertiary$),$ vinyl or aryl halides:
$\ce{CH_3C(C_2H_5)_2CH_2Br}.$
Which of the compounds will react faster in $S_N1$ reaction with the $–OH$ ion?
$\text{CH}_3-\text{CH}_2-\text{Cl}$ or $\text{C}_6\text{H}_5-\text{CH}_2-\text{Cl}$
Name the following halides according to $\text{IUPAC}$ system and classify them as alkyl, allyl, benzyl $($primary, secondary, tertiary$),$ vinyl or aryl halides: $\ce{CH_3CH(CH_3)CH(Br)CH_3}.$