Kumada Coupling:1. m-Diisobutylbenzene below could hypothetically be synthesized by Friedel-Crafts reaction. Write out the reaction with amechanism and give two reasons why you would NOT get the desired product.Draw the reaction (NOT a mechanism) for a Kumada coupling to produce the molecule above from m-dichlorobenzene.Calculate the theoretical yield for the reaction in question 2 using 1.5 g of p-dichlorobenzene and 3.0 mL isobutyl bromide.What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? Whatother impurities are present in your product and how do you know?

1. Friedel-Crafts Reaction and ChallengesReaction Mechanism:The synthesis of m-diisobutylbenzene via…

Answered: Kumada Coupling: 1. m-Diisobutylbenzene…

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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This CAN NOT be hand-drawn. Please type out all explanations. Please utilize a computer program to illustrate any examples! Thank you. Please answer 2C Write the separation scheme for the isolate the product, diphenylmethanol, from the reaction mixture after the reaction is complete.
This CAN NOT be hand-drawn. Please type out all explanations. Please utilize a computer program to illustrate any examples! Thank you.
CANNOT BE HAND-WRITTEN
Please solve question 2 and explain
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Friedel-Crafts Reaction: 8.00 grams of benzoyl chloride is reacted with ethanol under heated conditions. What amount (in grams) of the ethanol is required for the reaction and what is the theoretical yield of the ethyl benzoate product? Include a balanced equation.
what is the best way to come up with how to synthesize carboxylic acid , oct-4-yne to butanoic acid, or trans cyclodecene to decanedoic acid . I keep getting confused on how to go from the reactants to product, even with the amines. i can't figure out what to use to get to the product. Please explain Grignard rx as well.
Illustrate the reaction mechanism for the ethylation of p-cyclopropylphenol (other reactants: AlCI3 and ethylchloride). Refer to Friedel-Craft Alkylation mechanism as your guide in doing this mechanism. Show ALL partial charges in the EACH structure using BLUE ink. Arrows should be written using RED ink.
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The compound below is treated with W-bromosuccinimide (NBS) in the presence of light. Draw both resonance structures for the radical produced by reaction of the compound with a bromine atom. Assume reaction occurs only at the weakest C-H bond. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. Separate resonance structures using the ↔ symbol from the drop-down menu. • Include all valence radical electrons in your answer. Y ? #[ ] در

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