Which one is a nucleophilic substitution reaction among the following?
- A$CH_3-CH=CH_2 + H_2O \xrightarrow{H^{+}} CH_3-CH(OH)-CH_3$
- B$RCHO + R'MgX \to R-CH(OMgX)-R'$
- C$CH_3-CH_2-CH(CH_3)-CH_2Br + NH_3 \to CH_3-CH_2-CH(CH_3)-CH_2NH_2 + HBr$
- D$CH_3CHO + HCN \to CH_3CH(OH)CN$
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Similar Questions
The order of reactivity of the following compounds towards dilute aqueous $KOH$ in $SN_1$ reaction is
$I$. $CH_3CH_2CH_2CH_2Br$
$II$. $CH_3CH_2CHBrCH_3$
$III$. $(CH_3)_2CHCH_2Br$
$IV$. $(CH_3)_3CBr$
$I$. $CH_3CH_2CH_2CH_2Br$
$II$. $CH_3CH_2CHBrCH_3$
$III$. $(CH_3)_2CHCH_2Br$
$IV$. $(CH_3)_3CBr$
Explain the factors affecting $S_{N}1$ reaction.
Medium
View SolutionTertiary alkyl halides are practically inert to $SN^2$ mechanism because of....
Medium
View SolutionPredict all the alkenes that would be formed by dehydrohalogenation of the following halides with sodium ethoxide in ethanol and identify the major alkene:
$(i)$ $1-$Bromo$-1-$methylcyclohexane
$(ii)$ $2-$Chloro$-2-$methylbutane
$(iii)$ $2,2,3-$Trimethyl$-3-$bromopentane.
$(i)$ $1-$Bromo$-1-$methylcyclohexane
$(ii)$ $2-$Chloro$-2-$methylbutane
$(iii)$ $2,2,3-$Trimethyl$-3-$bromopentane.
Easy
View SolutionMost reactive for $S_{N}1$ reaction is
Medium
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