Theoretically it is possible for other isomers of the di-alkylated product to be formed. what are these two other isomers (structure and name)? Can you think of a reasonable explanation for why these products are not formed? Reaction: forming 1,4 di-t-butyl-2,5 –dimethoxybenzene through Friedel-Crafts alkylation using 1,4-dimethoxybenze, tert-butyl alcohol and sulfuric acid (the Lewis acid catalyst).

odds are decent that your handwriting right now looks a little bit different than it did five years ago, and will look different again in five more. when i look back through my notebooks from middle school to now, i see a long, slow progression from meticulous and teeny letters to bigger, sloppier ones, plus a few side detours: sometime in high school, for example, i decided those loopy cursive lowercase f’s were just the coolest, adopting them as the lone rep for cursive in my otherwise all-print handwriting.

explanation:

the atomic mass is the bottom number on the element.

-steel jelly

the answer is c i took the test