Which among the following statements is $NOT$ correct about $SN^2$ reaction mechanism?
- ANucleophile attacks the atom from the side opposite to halogen.
- BRate of reaction is dependent on the concentration of nucleophile.
- CBond formation and bond breaking occurs simultaneously.
- D$SN^2$ mechanism is observed in tertiary alkyl halides.
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Similar Questions
The major product obtained from the reaction of $2$-bromopentane with potassium ethoxide in ethanol is ....................
Medium
View SolutionThe rate of $S_N2$ reaction will be negligible in:
Medium
View SolutionWhich among the following halides will generate the most stable carbocation in a nucleophilic substitution reaction?
Which one of the following has the highest boiling point?
Match the following:
Reactants Products $A$. $C_2H_5Cl$,moist $Ag_2O$ $I$. $CH_3CH_2ONO$ $B$. $C_2H_5Cl$,aqueous ethanolic $AgCN$ $II$. $C_2H_4$ $C$. $C_2H_5Cl$,aqueous ethanolic $AgNO_2$ $III$. $CH_3CH_2OH$ $D$. $C_2H_5Cl$,ethanolic $KOH$ $IV$. $CH_3CH_2NC$
The correct match is:
| Reactants | Products |
|---|---|
| $A$. $C_2H_5Cl$,moist $Ag_2O$ | $I$. $CH_3CH_2ONO$ |
| $B$. $C_2H_5Cl$,aqueous ethanolic $AgCN$ | $II$. $C_2H_4$ |
| $C$. $C_2H_5Cl$,aqueous ethanolic $AgNO_2$ | $III$. $CH_3CH_2OH$ |
| $D$. $C_2H_5Cl$,ethanolic $KOH$ | $IV$. $CH_3CH_2NC$ |
The correct match is:
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