draw the resonance structure of the three possible carbocation intermediate to show how methoxyl (-OCH3) diects bromination toward ortho and para position

See explanation and image attached

Explanation:

We know that some substituted benzene reacts faster than benzene towards electrophillic substitution. This is often due to the activation of the benzene ring towards electrophillic substitution by resonance.

-OCH3 directs an incoming electrophile (such as during bromination) to the ortho or para position. This is made possible by resonance (mesomeric) effect as shown in the image attached to this answer.

Image credit: pinterest

here is table 2-2:

country

percent of eligible voters that voted

rank

united states

44.9%

138

canada

60.1%

107

costa rica

84.6%

14

hungary

66.9%

82

japan

57.0%

118

egypt

27.7%

159

south africa

85.5%

10

ans is no, the data set cannot be plotted as a single circle graph