10. For the following, use ONLY reactions we have studied in class. a) Write out 6 completely different reactions of acetophenone (reagent, product). b) Write out 3 preparations of 2-methyl-2-butanola different starting material for each one. You may use preps where you just change the functional group, and/or preps where you have to construct the carbon chain. c) Write out 3 preparations of pentanoic acid, a different starting material for each one. You may use preps where you just change the functiona group, and/or preps where you have to construct the carbon chain.

10. For the following, use ONLY reactions we have studied in class. a) Write out 6 completely different reactions of acetophenone (reagent, product). b) Write out 3 preparations of 2-methyl-2-butanola different starting material for each one. You may use preps where you just change the functional group, and/or preps where you have to construct the carbon chain. c) Write out 3 preparations of pentanoic acid, a different starting material for each one. You may use preps where you just change the functiona group, and/or preps where you have to construct the carbon chain.

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...

See similar textbooks

Similar questions

I do not understand how to work out this problem.
pls help, and circle the answer
None
answer A, B, & C. Skip #12
[Review Topics] Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol below. OH H • You do not have to consider stereochemistry. • Draw the enolate nucleophile in its carbanion form. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate multiple reactants using the + sign from the drop-down menu. 99.85 26924 10-√ Y ? [References] ChemDoodle #[ ] کر
help me please
Need help solving this, please show your work with the answer!
4. (10 points) Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible answer. LDA lodomethane CH3 H H
Draw the structure(s) of the major organic product(s), including counterions, of the following reaction. HBr H₂O You do not have to consider stereochemistry. • Include counter-ions, e.g., Na*, I, in your submission, but draw them in their own separate sketcher. • If no reaction occurs, draw the organic starting material. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. ⚫ Separate multiple products using the + sign from the drop-down menu. n [F F
Please help, i need fast answer. Please don't provide handwritten solution ....