Question

extra credit orgo chem

NaBH MOH 1.Write two starting materials (five or fewer C's) that react to form the target molecule starting from any carbonyl compound and any organometallic reagent. OH Part IV. Mechanistic Puzzlers (16 pts) 10. Reduction of cyclohexanone using lithium aluminum hydride gives a deuterated alcohol when D.O is used instead of H.O in the workup step. Account for this outcome with a mechanism, showing curved arrows, the key intermediate, and lone pairs and charges. (6 pts) 1. LiAIHA 2. D.0 11. Write the mechanism for hydrolysis of an ester under acidic conditions. (10 pts) Draw all intermediates, lone pairs and charges, equilibrium arrows, and especially curved arrows to indicate electron flow. Hint: the sequential steps are protonation, nucleophilic attack, proton transfer, loss of water, and deprotonation. H+, H20 OH + CH, OH 2H0 VH

Answer 1

mechanismen CH) re eveningen A utoriul se many s ů) Carbonyl.compound » cao organometalic comp 7 (4=cy-142 Mg BV mechanism t .641=cy-en, mer c=0 2 -c-uzum to ho do on--- PART@_mechanishic puzzlers (10) CASA noe An 7 I-CH₂O -- م و of these ther- coocny Zanester e Carbonylic Acid

PART ID) mutigtep MAROH : DH 19 okrem cesta este o LAN strom 031211 mo -Professor ning Mul
all answer is given plz give up thumb for rating.