Answer each question using the ball-and-stick model of compound A. a. Give the IUPAC name for A, including R,S designations for stereogenic centers. b. Classify A as a 1°, 2°, or 3° alcohol. c. Draw a stereoisomer for A and give its IUPAC name. d. Draw a constitutional isomer that contains an OH group and give its IUPAC name. e. Draw a constitutional isomer that contains an ether and give its IUPAC name. f. Draw the products formed (including stereochemistry) when A is treated with each reagent: [1] NaH; [2] H2SO4; [3] POCI,, pyridine; [4] HCl; [5] SOCI, pyridine; [6] TSCI, pyridine. A

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Answer each question using the ball-and-stick model of compound A.
a. Give the IUPAC name for A, including R,S designations for stereogenic centers.
b. Classify A as a 1°, 2°, or 3° alcohol.
c. Draw a stereoisomer for A and give its IUPAC name.
d. Draw a constitutional isomer that contains an OH group and give its IUPAC name.
e. Draw a constitutional isomer that contains an ether and give its IUPAC name.
f. Draw the products formed (including stereochemistry) when A is treated with each reagent:
[1] NaH; [2] H2SO4; [3] POCI,, pyridine; [4] HCl; [5] SOCI, pyridine; [6] TSCI, pyridine.
A
Transcribed Image Text:Answer each question using the ball-and-stick model of compound A. a. Give the IUPAC name for A, including R,S designations for stereogenic centers. b. Classify A as a 1°, 2°, or 3° alcohol. c. Draw a stereoisomer for A and give its IUPAC name. d. Draw a constitutional isomer that contains an OH group and give its IUPAC name. e. Draw a constitutional isomer that contains an ether and give its IUPAC name. f. Draw the products formed (including stereochemistry) when A is treated with each reagent: [1] NaH; [2] H2SO4; [3] POCI,, pyridine; [4] HCl; [5] SOCI, pyridine; [6] TSCI, pyridine. A
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