(C) In the given reaction,the bromine atom $(-Br)$ in tert-butyl bromide is replaced by a hydroxyl group $(-OH)$ from water. Since the incoming group

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(C) In the given reaction,the bromine atom $(-Br)$ in tert-butyl bromide is replaced by a hydroxyl group $(-OH)$ from water. Since the incoming group is a nucleophile $(-OH^-)$,this is a nucleophilic substitution reaction. Specifically,it follows an $S_N1$ mechanism because the substrate is a tertiary alkyl halide.

Class 12 Chemistry Haloalkanes and Haloarenes Properties of Haloalkanes

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The following reaction,$(CH_3)_3CBr + H_2O \rightarrow (CH_3)_3COH + HBr$,is an example of:

MHT CET 2008 All MHT CET

A
elimination reaction
B
free radical substitution
C
nucleophilic substitution
D
electrophilic substitution

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Class 12

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Haloalkanes and Haloarenes

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Properties of Haloalkanes

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The arrangement of the following compounds in the increasing order of their boiling points is:
$i$. bromomethane
$ii$. bromoform
$iii$. chloromethane
$iv$. dibromomethane

MediumKCET 2015

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When chloroform is treated with excess oxygen,it forms:

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Which of the following isomers of $C_4H_9Br$ is a chiral molecule?

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Which of the following compounds would undergo $S_N1$ reaction faster and why?
$(A)$ Cyclohexylmethyl chloride
$(B)$ Benzyl chloride

Medium

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The conversion of ethyl bromide to ethyl iodide using sodium iodide and dry acetone is known as:

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The following reaction,$(CH_3)_3CBr + H_2O \rightarrow (CH_3)_3COH + HBr$,is an example of:

Similar Questions

The arrangement of the following compounds in the increasing order of their boiling points is:$i$. bromomethane$ii$. bromoform$iii$. chloromethane$iv$. dibromomethane

When chloroform is treated with excess oxygen,it forms:

Which of the following isomers of $C_4H_9Br$ is a chiral molecule?

Which of the following compounds would undergo $S_N1$ reaction faster and why?$(A)$ Cyclohexylmethyl chloride$(B)$ Benzyl chloride

The conversion of ethyl bromide to ethyl iodide using sodium iodide and dry acetone is known as:

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The arrangement of the following compounds in the increasing order of their boiling points is:
$i$. bromomethane
$ii$. bromoform
$iii$. chloromethane
$iv$. dibromomethane

Which of the following compounds would undergo $S_N1$ reaction faster and why?
$(A)$ Cyclohexylmethyl chloride
$(B)$ Benzyl chloride