Statement -1 : Rate of S(N)1 reaction ...

Statement -1 : Rate of `S_(N)1` reaction is faster than that of `S_(N)2` reaction
Statement -2 : `S_(N)2` reaction is favoured by polar aprotic solvent
Statement -3 : `S_(N)1` reaction involves racemization

TTT

FFT

FTT

TFT

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S_(N)1 reaction is faster in

`CH_(3)CH_(2)Cl`

`CH_(3)-overset(CH_(3))overset(|)underset(CH_(3))underset(|)(C)-Cl`

`CH_(3)-underset(CH_(3))underset(|)underset(CH_(2))underset(|)underset(|)(CH)-Cl`

Non-polar solvent

More no of alkyl group on the carbonv atom

Small groups on the carbon attached to the halogen atom

None of these

Non - polar solvents

Bulky alkyl groups on the carbon atom attached to halogen atom

Less steric hindrance containing akyl halides

Less stable carbocation