The only alcohol that can be prepared by the | vedclass

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Question

(A) The indirect hydration of alkenes involves the reaction with concentrated $H_2SO_4$ followed by hydrolysis.$CH_2=CH_2 + H_2SO_4 	o CH_3-CH_2-HSO_

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Ethyl alcohol

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(A) The indirect hydration of alkenes involves the reaction with concentrated $H_2SO_4$ followed by hydrolysis.$CH_2=CH_2 + H_2SO_4 	o CH_3-CH_2-HSO_4 \xrightarrow{H_2O, \Delta} CH_3-CH_2OH + H_2SO_4$Since the addition of $H_2SO_4$ to alkenes follows Markownikoff's rule,the hydrogen atom attaches to the carbon with more hydrogen atoms,and the $-HSO_4$ group attaches to the more substituted carbon.For ethene $(CH_2=CH_2)$,this results in the formation of ethanol $(CH_3-CH_2OH)$.For higher alkenes,this method typically yields secondary or tertiary alcohols. Therefore,ethyl alcohol is the only primary alcohol that can be prepared by this method.

The only alcohol that can be prepared by the indirect hydration of alkene is

Similar Questions

Propan-$1$-ol can be prepared from propene by:

What are $X$ and $Y$ in the following reactions?
$CH_2O \xrightarrow[(ii) H_3O^+]{(i) X} CH_3(CH_2)_2CH_2OH$
$Y \xrightarrow[(ii) H_3O^+]{(i) C_2H_5MgBr} CH_3CH_2C(CH_3)_2OH$

Show how will you synthesize:
$(i)$ $1-$phenylethanol from a suitable alkene.
$(ii)$ cyclohexylmethanol using an alkyl halide by an $S_{N}2$ reaction.
$(iii)$ pentan$-1-$ol using a suitable alkyl halide?

Explain the methods of preparing alcohols from carbonyl compounds using Grignard reagents.

Which of the following reagents is $NOT$ useful for the preparation of alkyl chloride from alcohol?

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