$E 1$ mechanism readily occur in $3^{\circ}$ carbocation. Presence of higher alkyl groups in alkyl halide also favours $E 1$ mechanism.
The neopentyl halide in ethanol yields alkenes by $E 1$ mechanism due to steric factor which prevents E2 mechanism. In $E 1$ mechanism, Heterolytic dissociation of alkyl halide followed by abstraction of proton by base from a $C$ adjacent to the positively
charged $C$ atom $(\beta-C$ atom $)$, takes place as follows: