1. (a) Formulate four(4) different ways to synthesize 3-methylhexane from any readily available starting material. For each of these, show the reagent(s)required for each transformation, including all intermediates. (b) H.C. Brown used ester (2A) to test a new reducing agent which did indeed form alcohol (2B). How might he have made the ester (2A) from benzene. 2A C₂Me NaBH AICI3 2B CH₂OH (c) Suggest synthesis for the target molecules (3A) and (3B) needed as intermediates. TM (3A) in the synthesis of brominated hydroxybenzoic acids and TM (3B) in the synthesis of model compounds for studying biological mechanisms of ester hydrolysis. CO₂ OH CHO O₂N Br JL

1. (a) Formulate four(4) different ways to synthesize 3-methylhexane from any readily available starting material. For each of these, show the reagent(s)required for each transformation, including all intermediates. (b) H.C. Brown used ester (2A) to test a new reducing agent which did indeed form alcohol (2B). How might he have made the ester (2A) from benzene. 2A C₂Me NaBH AICI3 2B CH₂OH (c) Suggest synthesis for the target molecules (3A) and (3B) needed as intermediates. TM (3A) in the synthesis of brominated hydroxybenzoic acids and TM (3B) in the synthesis of model compounds for studying biological mechanisms of ester hydrolysis. CO₂ OH CHO O₂N Br JL

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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