Chapter 12, Problem 12.70E

The reaction of phenylmagnesium bromide (C6H5MgBr) with propanal (CH3CH2CHO)3 followed by hydrolysis yields.  A. 2-phenyl-1-propanol B. 1-phenyl-1propanol C. 3-phenyl-2-propanol D. 3-phenyl-1-propanol   Why is the correct answer B? Please explain what is happening. Please include a detailed explanation and/or a drawing of steps needed to understand the reaction or question.

What is the product of the reaction sequence below? Why is the correct answer D? Please explain what is happening. Please include a detailed explanation and a drawing of steps needed to understand the reaction or question.    The part that is under the pen in the image is (1) CH3CHO (2) H3O+

What is the missing reactant in this organic reaction? R+ OH HD CH3-CH2-CH-CH3 H A CH3 CH3-CH2-C-O-CH-CH2-CH3 + H₂O Specifically, in the drawing area below draw the condensed structure of R. If there is more than one reasonable answer, you can draw any one of them. If there is no reasonable answer, check the No answer box under the drawing area. No answer Click anywhere to draw the first atom of your structure. ☐ : Jm +

Draw the major product of the following E2 reaction. Make sure you pay attention to REGIOCHEMISTRY and STEREOCHEMISTRY. Explain why this product is formed using 10 words or less for each. (a) NaH Br acetone TSO, NaH (b) acetone

2. Circle the compound that will react SLOWER in an E2 reaction. To get credit for this question, you must EXPLAIN how you got your answer using STRUCTURES and WORDS. Br ** Br...

8. 2 20 00 Draw ALL of the possible products for the following reaction CIRCLE the MAJOR product NaOMe MeOH

NAME: 1. Draw the major product of the following E2 reaction. Make sure you pay attention to REGIOCHEMISTRY and STEREOCHEMISTRY. To get credit for this question, you must EXPLAIN how you got your answer using STRUCTURES and WORDS. Br NaOCH3 acetone F2 reaction To get credit for this

3. Reactions! Fill in the information missing below. Make sure to pay attention to REGIOCHEMISTRY and STEREOCHEMISTRY. Br2 CH3OH + 4. Mechanism! Show the complete arrow pushing mechanism, including all steps and intermediates for the following reactions. To get credit for this, you MUST show how ALL bonds are broken and formed, using arrows to show the movement of electrons. H3O+ HO

Please provide a synthesis for the Ester using proponoic acid, thank you!