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