CHEMISTRY: AN INTRODUCTION TO GENERAL, O
13th Edition
ISBN: 9780137444298
Author: Timberlake
Publisher: PEARSON
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Textbook Question
Chapter 12, Problem 12.67CP
Compound A is a primary alcohol whose formula is C3H8O. When compound A is heated with strong acid, it dehydrates to form compound B (C3H6). When compound A is oxidized, compound C (C3H60) forms. Draw the condensed structural formulas and give the IUPAC names for compounds A, B, and C. (12.3, 12.4)
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12.60 Which of the following aldehydes or ketones are soluble in
water? (12.3)
|3|
a. CH3-CH2 -C-CH3
b. CH3 — С —н
CH3
c. CH3-CH2-CH-CH2-CH2-C-H
12.52 Draw the condensed structural or line-angle formula for the
alkene, aldehyde, or ketone product of each of the following
reactions: (12.4)
H, heat
a.
ОН
CH; OH
b. CHз — СH — СH-CH,
OH
[0]
ОН
d. CH3-CH2-CH2-CH-CH3
(12.3)Which of the following has the strongest dispersion force between its molecules?
O CH3CH3
O CH3CH₂CH₂CH₂CH3
O All of these have the dispersion forces with the same strength.
O CH3CH₂CH₂CH3
O CH3CH₂CH₂CH₂CH₂CH3
Chapter 12 Solutions
CHEMISTRY: AN INTRODUCTION TO GENERAL, O
Ch. 12.1 - Give the IUPAC name for each of the following: a....Ch. 12.1 - Give the IUPAC name for each of the following: a....Ch. 12.1 - Prob. 12.3PPCh. 12.1 - Draw the condensed structural formula, or...Ch. 12.1 - Give the common name for each of the following: a....Ch. 12.1 - Prob. 12.6PPCh. 12.1 - Draw the condensed structural formula, or...Ch. 12.1 - Draw the condensed structural formula, or...Ch. 12.2 - Classify each of the following alcohols as primary...Ch. 12.2 - Classify each of the following alcohols as primary...
Ch. 12.2 - Prob. 12.11PPCh. 12.2 - Prob. 12.12PPCh. 12.2 - Give an explanation for each of the following...Ch. 12.2 - Give an explanation for each of the following...Ch. 12.3 - Identify each of the following compounds as an...Ch. 12.3 - Identify each of the following compounds as an...Ch. 12.3 - Give the common name for each of the following: a....Ch. 12.3 - Give the common name for each of the following: a....Ch. 12.3 - Give the IUPAC name for each of the following: a....Ch. 12.3 - Give the IUPAC name for each of the following: a....Ch. 12.3 - Draw the condensed structural formula for each of...Ch. 12.3 - Draw the condensed structural formula for each of...Ch. 12.3 - Which compound in each of the following pairs...Ch. 12.3 - Which compound in each of the following pairs...Ch. 12.4 - Write the balanced chemical equation for the...Ch. 12.4 - Write the balanced chemical equation for the...Ch. 12.4 - Prob. 12.27PPCh. 12.4 - Draw the condensed structural or line-angle...Ch. 12.4 - Draw the condensed structural or line-angle...Ch. 12.4 - Draw the condensed structural or line-angle...Ch. 12.4 - Draw the condensed structural formulas for the...Ch. 12.4 - Draw the condensed structural formulas for the...Ch. 12.4 - Prob. 12.33PPCh. 12.4 - Prob. 12.34PPCh. 12.4 - Oxybenzone is an effective sunscreen whose...Ch. 12.4 - Avobenzone is a common ingredient in sunscreen....Ch. 12 - Prob. 12.37UTCCh. 12 - The compound frambinone has the taste of...Ch. 12 - A compound called resveratrol is an antioxidant,...Ch. 12 - A compound called cinnamaldehyde is found in...Ch. 12 - Prob. 12.41UTCCh. 12 - Prob. 12.42UTCCh. 12 - Prob. 12.43APPCh. 12 - Classify each of the following alcohols as primary...Ch. 12 - Give the IUPAC name for each of the following...Ch. 12 - Give the IUPAC name for each of the following...Ch. 12 - Draw the condensed structural or line-angle...Ch. 12 - Draw the condensed structural or line-angle...Ch. 12 - Which compound in each pair would be more soluble...Ch. 12 - Which compound in each pair would be more soluble...Ch. 12 - Draw the condensed structural or line-angle...Ch. 12 - Draw the condensed structural or line-angle...Ch. 12 - Draw the condensed structural or line-angle...Ch. 12 - Draw the condensed structural or line-angle...Ch. 12 - Give the IUPAC name for each of the following:...Ch. 12 - Give the IUPAC name for each of the following:...Ch. 12 - Draw the condensed structural or line-angle...Ch. 12 - Draw the condensed structural or line-angle...Ch. 12 - Which of the following aldehydes or ketones are...Ch. 12 - Which of the following aldehydes or ketones are...Ch. 12 - Draw the condensed structural or line-angle...Ch. 12 - Draw the condensed structural or line-angle...Ch. 12 - Prob. 12.63CPCh. 12 - Draw the condensed structural formulas and give...Ch. 12 - A compound with the formula C4H8O is synthesized...Ch. 12 - A compound with the formula C5H10O oxidizes to...Ch. 12 - Compound A is a primary alcohol whose formula is...Ch. 12 - Compound X is a secondary alcohol whose formula is...Ch. 12 - Prob. 21CICh. 12 - Prob. 22CICh. 12 - Prob. 23CICh. 12 - Prob. 24CICh. 12 - Prob. 25CICh. 12 - lonone is a compound that gives violets their...
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- 12.38 The compound frambinone has the taste of raspberries and has been used in weight loss. Identify the functional groups in frambinone. (12.1, 12.3) HO O CH,—CH,—C–CH3 14 Frambinone odioarrow_forward12.42 Which of the following will give a positive Tollens' test? (12.4) 1-propanol b. 2-propanol c. hexanal a.arrow_forward(12.9) Which of the following has the highest boiling point? O Both H₂S and H₂O have the same boiling point that is higher than the boiling point of H₂Se. O H₂Se O H₂O O H₂Sarrow_forward
- Kindly give the IUPAC names of the following alcohol compounds: 1. 2. 3. 4. 5. OH (CH₂)₂CHCH₂CH(CH₂CH₂CH(OH)CH₂CH₂ H₂CO LOCH, SHarrow_forward12.26 Write the balanced chemical equation for the complete combustion of each of the following compounds: a. 1-propanol b. 3-hexanolarrow_forward12.28 Draw the condensed structural or line-angle formula for the alkene produced by each of the following dehydration reactions: a. CH3 CH₂-OH b. C. OH OH Ht, heat Ht, heat H, heatarrow_forward
- What is the IUPAC name of the following compound? O bicyclo[6.5.4]undecane bicyclo[4.3.2]nonane [4.3.2]bicyclononane O [2.3.4]bicycloundecane O bicyclo[4.3.2]undecane Aarrow_forward11.25 Give the IUPAC name for each of the following: a. H₂C=CH₂ b. d. CH₂ CH₂-C=CH₂ CH₁ CH₂-C=C-CH,arrow_forward12.31 Write the IUPAC name for each of the following, using cis or trans prefixes, if needed: a. b. C. CH3-CH₂ H H H c=c C=C CH3 H H CH₂-CH₂-CH₂ - CH₂arrow_forward
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