CNCT ORG CHEM 6 2020
6th Edition
ISBN: 9781266807244
Author: SMITH
Publisher: MCG
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Textbook Question
Chapter 18, Problem 41P
Give the structure corresponding to each name.
a.
b.
c.
d.
e.
f.
g.
h.
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Give the structure corresponding to each name.
a. 7,7-dimethyl-4-octanol
b. 5-methyl-4-propyl-3-heptanol
c. 2-tert-butyl-3-methylcyclohexanol
d. trans-1,2-cyclohexanediol
Draw the structure corresponding to each name.
a. 3,3-dimethylpentanoic acid
b. 4-chloro-3-phenylheptanoic acid
c. (2R)-2-chloropropanoic acid
d. B,B-dichloropropionic acid
e. m-hydroxybenzoic acid
f. o-chlorobenzoic acid
i. 2,2-dichloropentanedioic acid
j. 4-isopropyl-2-methyloctanedioic acid
g. potassium acetate
h. sodium a-bromobutyrate
Cyclopentanone is treated with chlorine (Cl2) in the presence of acid (H*).
What product is formed?
A. Chlorocyclopentane
B. 1-chloro-1-hydroxycyclopentane
C. 2-chlorocyclopentanone
D. 3-chlorocyclopentanone
Chapter 18 Solutions
CNCT ORG CHEM 6 2020
Ch. 18.1 - Rank the following compounds in order of...Ch. 18.1 - Prob. 2PCh. 18.2 - Give the IUPAC name for each aldehyde.Ch. 18.2 - Prob. 4PCh. 18.2 - Give the IUPAC name for each ketone.Ch. 18.5 - Prob. 11PCh. 18.9 - Problem 21.17 Draw the products of the following...Ch. 18.9 - Problem 21.18 Outline a synthesis of each Wittig...Ch. 18.9 - Problem 21.19 Draw the products (including...Ch. 18.9 - Problem 21.20 What starting materials are needed...
Ch. 18.9 - Prob. 19PCh. 18.10 - Problem 21.22 The product formed when reacts with...Ch. 18.10 - Prob. 21PCh. 18.11 - Prob. 22PCh. 18.11 - Prob. 23PCh. 18.11 - Prob. 24PCh. 18.12 - Prob. 25PCh. 18.12 - Problem 21.28 Draw a stepwise mechanism for the...Ch. 18.13 - Problem 21.29 Draw the products of each...Ch. 18 - Problem 21.40 (a) Give the IUPAC name for A and B....Ch. 18 - 21.41 Rank the following compounds in order of...Ch. 18 - Prob. 39PCh. 18 - 21.43 Give the IUPAC name for each compound.
a....Ch. 18 - 21.44 Give the structure corresponding to each...Ch. 18 - Prob. 42PCh. 18 - 21.46 Draw the products of each reaction.
a. e....Ch. 18 - Prob. 44PCh. 18 - 21.48 Draw all stereoisomers formed in each...Ch. 18 - Prob. 54PCh. 18 - Prob. 55PCh. 18 - Prob. 56PCh. 18 - Devise a synthesis of each alkene using a Wittig...Ch. 18 - Prob. 60PCh. 18 - Prob. 62PCh. 18 - Prob. 63PCh. 18 - 21.64 Draw a stepwise mechanism for the following...Ch. 18 - 21.65 Draw a stepwise mechanism f or the following...Ch. 18 - Prob. 67PCh. 18 - 21.67 Draw a stepwise mechanism for each...Ch. 18 - Prob. 69PCh. 18 - Prob. 70P
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- Give the structure corresponding to each name. a. butyl ethyl ketone c. p-ethylacetophenone b. 2-methyl-3-pentanone d. 2-propylcyclobutanonearrow_forwardDraw the structure corresponding to each name. a. 2-hydroxyheptanoic acid b. 4-chlorononanoic acid c. 3,4-dibromobenzoic acid d. lithium propanoate e. 2,2-dibromobutanoic acid f. ethyl 2-methylpropanoatearrow_forwardWhat is the name for this compound? Select one: a. 2-bromo-5-ethylphenol b. 4-bromo-1-ethyl-5-phenol c. 6-bromo-3-ethylphenol d. 2-bromo-5-ethylcyclohexanol e. 2-bromo-5-methylphenolarrow_forward
- B. Draw structures corresponding to the following names. 1. 3-methylbutanal 7. 4-chloro-2-pentanone 2. o-hydroxybenzoic acid 8. phenylacetaldehyde 3. 3-chloro-4-cyanopentanoic acid 9. cis-3-tert-butylcyclohexanecarbaldehyde 4. 3-methyl-3-butenal 10. 2-(1-chloroethyl)-5-methylheptanal 5. 2,3-dimethylhexanoic acid 11. trans-1,2-cyclobutanedicarboxylic acid 6. 2-hexen-4-ynoic acid 12. heptanedioic acidarrow_forward4. Which compound is an acetal? O. %3D a. I b. II с. III d. IV e. All of thesearrow_forwardInstructions: Give the IUPAC name for each compound. A. CH₂ CH₂CH₂CH₂CCH₂COOH CH₂ B. CH.CHCHCH.COOH a CH₂CH₂ C. (CH,CH,), CHCH,CH COOH Instructions: Give the structure corresponding to each IUPAC name. a. 2-bromobutanoic acid b. 2,3-dimethylpentanoic acid c. 2-ethyl-5,5-dimethyloctanoic acid d. 3,4,5,6-tetraethyldecanoic acidarrow_forward
- Nonearrow_forwardDraw the structure of the ff. aldehydes and ketones. a. 3-chlorobutanal 6. 8,8-dibromo -4-cthylcyclo hexanone C. 2,4-dimetnylpontanone • Draw the structure of the ff. compounds. a. oyclobutanecarboxylic acid b. 3,8-dimcthylpontancdioic acid C. 4-aminopcntanoic acid d. 2-mothylcycloheranecarooxylic acid m- chlorobėnzoic acidarrow_forwardstructure onlyarrow_forward
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