Chapter 12: PROBLEM 12.33 (page 487)
Question: Draw the organic products formed when each alkene is treated with H2 / Pd-C. Indicate the three-dimensional structure of all stereoisomers formed.
a.
b.
c.
Short Answer
Answer
a.
b.
c.
Chapter 12: PROBLEM 12.33 (page 487)
Question: Draw the organic products formed when each alkene is treated with H2 / Pd-C. Indicate the three-dimensional structure of all stereoisomers formed.
a.
b.
c.
Answer
a.
b.
c.
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Question: The Birch reduction is a dissolving metal reaction that converts substituted benzenes to cyclohexa-1,4-dienes using Li and liquid ammonia in the presence of an alcohol. Draw a stepwise mechanism for the following Birch reduction.
Question: Draw all stereoisomers formed when each alkene is treated with mCPBA.
a.
b.
c.
Question: Draw the organic products formed when allylic alcohol A is treated with each reagent.
a. H2 +Pd-c
b. mCPBA
c. PCC
d. CrO3 ,H2SO4, H2O
e.(CH3)3COOH , Ti [OCH(CH3)3]4 (+) -DET
f.(CH3)3COOH , Ti [OCH(CH3)3]4 (-) -DET
g. [1] PBr3,[2] LiAlH4 ,[3] H2O
h. HCrO4- –Amberlyst A-26 resin
Question:Devise a synthesis of each compound from acetylene and any other required reagents.
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