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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Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 7E

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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] POCl3, pyridine; [4] HCl; [5] SOCl2, pyridine; [6] TsCl, pyridine
Draw the eight constitutional isomers having the molecular formula C5H11Cl. a.Give the IUPAC name for each compound (ignoring R and S designations). b.Classify each alkyl halide as 1°, 2°, or 3°. c.Label any stereogenic centers. d.For each constitutional isomer that contains a stereogenic center, draw all possible stereoisomers, and label each stereogenic center as R or S.
Give the IUPAC name for each compound. CH3 a. CH,CHCH-C CHO b. CH3 H CH2CH3
Answer each question using the ball-and-stick model of compound A. Draw a stereoisomer for A and give its IUPAC name.Draw a constitutional isomer that contains an OH group and give itsIUPAC name.
Answer each question for A and B depicted in the ball-and-stick models.a. What is the IUPAC name for each compound?b. What product is formed when each compound is treated with NaOH?c. Name the products formed in part (b).d. Draw the structure of an isomer that is at least 105 times less acidic than each compound.
1. Write the IUPAC name of each compound. a. Br b. C.
INSTRUCTION: Give the IUPAC name for each ketone. A. B. C. D. E. CH₂CH₂CCHCH₂CH₂CH₂ SCHICHS CH₂ CH3 (CH₂)2CCCH₂CH₂CH₂CH3 CH₂ INSTRUCTION: DRAW the structure corresponding to each name. A. butyl ethyl ketone B. 2-methyl-3-pentanone C. p-ethylacetophenone D. 2-propylcyclobutanone E. 2-cyclohexenone
1. Write IUPAC name for each structure below. a. CI b. Br d. نیومده e.
Give the IUPAC name for each ketone. C-CHCH,CH3 b. a.
Draw the following: 1. a. 3-methyl-1-butanethiol (skunk scent) b. triphenylmethanol c. 4-(bromomethyl)-3-octanol d. 3-cyclopentenethiol
a. b. Question 2: Give IUPAC name for each compound. o & C. d. 1 e. f.
B. Give the IUPAC name for each compound. a. b. d.

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