Question

Which ring position(s) of toluene are most reactive
toward electrophilic aromatic
substitution?
(a) ortho and para
(b) meta and para
(c) ortho and meta
(d) meta​

Answer 1

Answer:

c )ortho and meta

Explanation:

as Ch3 effect of toluene...will significantly increases the hyperconjugation effect on these positions...

so as an electophile- electrons loving comes to the o and p position...