A2. Complete the following by writing the structure of the principal organic product(s) for each step. If you believe no reaction will occur, write "No Reaction". Where relevant, clearly indicate the preferred stereochemistry of the product. (0) 1.DMSO LIAIH (COC) CH₂=CH₂=CH₂OH- 2. Et₂N (ii) H₂ Lindlar Catalyst n-Buli (2 Equiv.) HMPA, THF C10H21Br H₂O OH CBr4. (CeHs)P (iii) NH₂ CO₂H HONO

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A2. Complete the following by writing the structure of the principal organic
product(s) for each step. If you believe no reaction will occur, write "No
Reaction". Where relevant, clearly indicate the preferred stereochemistry of the
product.
(0)
1.DMSO
(COC)
LIAIH
CH₂=CH₂=CH₂OH
2. Et₂N
(ii)
n-Buli (2 Equiv.)
HMPA, THE
H₂ Lindlar Catalyst
C10H21Br
H₂O
OH
CBr4 (CH)P
(iii)
(iv)
NH₂
CO₂H
OH
HONO
1-BuOOH, TI(O/Pr)4
(-)-Diethyltartrate
CH₂Cl₂
Red-Al
Transcribed Image Text:A2. Complete the following by writing the structure of the principal organic product(s) for each step. If you believe no reaction will occur, write "No Reaction". Where relevant, clearly indicate the preferred stereochemistry of the product. (0) 1.DMSO (COC) LIAIH CH₂=CH₂=CH₂OH 2. Et₂N (ii) n-Buli (2 Equiv.) HMPA, THE H₂ Lindlar Catalyst C10H21Br H₂O OH CBr4 (CH)P (iii) (iv) NH₂ CO₂H OH HONO 1-BuOOH, TI(O/Pr)4 (-)-Diethyltartrate CH₂Cl₂ Red-Al
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