21.A researcher was asked to prepare butylbenzene from benzene. They chose to use chlorobutane and a Lewis acid catalyst (shown below), but was surprised to find that butylbenzene was not formed. butylbenzene? Provide a complete curved-arrow mechanism that accounts for the formation of the unwanted product. What isomeric product was formed instead of AIC butyl benzene not formed! undesired product After realizing their eror, the researcher was able to make butylbenzene from benzene in a multi-step process. Outline this synthetic sequence in the space below (no mechanisms, please).

21.A researcher was asked to prepare butylbenzene from benzene. They chose to use chlorobutane and a Lewis acid catalyst (shown below), but was surprised to find that butylbenzene was not formed. butylbenzene? Provide a complete curved-arrow mechanism that accounts for the formation of the unwanted product. What isomeric product was formed instead of AIC butyl benzene not formed! undesired product After realizing their eror, the researcher was able to make butylbenzene from benzene in a multi-step process. Outline this synthetic sequence in the space below (no mechanisms, please).

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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20:24 : E) 03 12. Fill in the box with the major organic product of the first step of the reaction shown? The first step of the reaction shown is an exhaustive methylation and is one of the SN2, SN1, E2, or E1 reactions. Another piece of information about this full reaction, the second step proceeds via an E2 mechanism. xs CH₂l 120, A 13. What is the name of the reaction in the previous question? A) Swern Oxidation B) Hofmann Elimination Cope Elimination Williamson Ether Synthesis Exam 1, Stage I 4 Send a chat O
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