In the current experiment, we will use a different electrophile (the tert.-butyl cation) to alkylate 1,4-dimethoxybenzene. This is a Friedel-Crafts Alkylation reaction. LOCH3 (H;C);C. LOCH3 (CH3);COH CH;COOH/H,SO4 H;CO H;COʻ `C(CH3)3

In the current experiment, we will use a different electrophile (the tert.-butyl cation) to alkylate 1,4-dimethoxybenzene. This is a Friedel-Crafts Alkylation reaction. LOCH3 (H;C);C. LOCH3 (CH3);COH CH;COOH/H,SO4 H;CO H;COʻ `C(CH3)3

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Question

I need an explanation on the mechanism, linked bellow

1 paragraph explanation on the steps and mechanism. and what the final product is called

In the current experiment, we will use a different electrophile (the tert.-butyl cation) to alkylate
1,4-dimethoxybenzene. This is a Friedel-Crafts Alkylation reaction.
LOCH3
(H;C);C,
LOCH3
(CH3);COH
CH;COOH/H,SO4
H;CO
H;CO
`C(CH3)3

The mechanism of the above reaction is:
(CH3);COH
+ H2SO4
(CH3);C-
+
HSO,
LOCH3
-H
(H3C);C
(CH3)3C
OCH3
H3CO
H;CO
H3C)3C.
LOCH3
(H3C);C.
LOCH3
(CH3);C-
H3CO
C(CH3)3
H3CO

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