 Solution

The primary chloride undergoes an SN2 reaction; the triphenylmethyl chloride undergoes an SN1 reaction. The primary site is accessible to back-side attack, whereas three phenyl groups make back-side attack at the triphenylmethyl site extremely hindered and stabilize its carbocation through resonance.

For the SN2 reaction, a suitable transition state isThe entering C and leaving Cl lie on opposite sides of the reacting carbon, with partial C–C and C–Cl bonds. The total charge is $-1$. This transition state is not a discrete reaction intermediate.

For the SN1 reaction, the approximately planar $\mathrm{P}{\mathrm{h}}_3{\mathrm{C}}^{+}$ carbocation is a genuine reaction intermediate. Assuming its formation by C–Cl heterolysis is rate determining and trapping is rapid,Thus the limiting rate law is independent of ethanol concentration. The successive attack and proton transfer occur after the slow ionization; a cation-stabilizing environment and efficient trapping underpin this idealized SN1 description.