Chemistry: An Introduction to General, Organic, and Biological Chemistry (13th Edition)
13th Edition
ISBN: 9780134421353
Author: Karen C. Timberlake
Publisher: PEARSON
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Textbook Question
Chapter 11, Problem 11.49APP
Give the IUPAC name (including cis or trans, if needed) for each of the following: (11.5, 11.6)
a. 
b.
C.
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Just answers to question 11.54
12.58 Draw the condensed structural or line-angle formula, if cyclic,
for each of the following: (12.3)
a. formaldehyde
c. 3-methyl-2-hexanone d. 3,5-dimethylhexanal
b. 2-chlorobutanal
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
Chapter 11 Solutions
Chemistry: An Introduction to General, Organic, and Biological Chemistry (13th Edition)
Ch. 11.1 - Identify each of the following as a formula of an...Ch. 11.1 - Identify each of the following as a formula of an...Ch. 11.1 - Identify each of the following properties as more...Ch. 11.1 - Identify each of the following properties as more...Ch. 11.1 - Prob. 11.5PPCh. 11.1 - Prob. 11.6PPCh. 11.2 - Give the IUPAC name for each of the following...Ch. 11.2 - Give the IUPAC name for each of the following...Ch. 11.2 - Draw the condensed structural formula for alkanes...Ch. 11.2 - Draw the condensed structural formula for alkanes...
Ch. 11.3 - Indicate whether each of the following pairs...Ch. 11.3 - Indicate whether each of the following pairs...Ch. 11.3 - Give the IUPAC name for each of the following a....Ch. 11.3 - Give the TUPAC name for each of the following: a....Ch. 11.3 - Draw the condensed structural formula for each of...Ch. 11.3 - Draw the condensed structural formula for each of...Ch. 11.3 - Draw the line-angle formula for each of the...Ch. 11.3 - Prob. 11.18PPCh. 11.4 - Heptane, used as a solvent for rubber cement, has...Ch. 11.4 - Nonane has a density of 0.79 g/mL and boils at 151...Ch. 11.4 - Write the balanced chemical equation for the...Ch. 11.4 - Write the balanced chemical equation for the...Ch. 11.5 - Identify the following as alkanes, alkenes,...Ch. 11.5 - Identify the following as alkanes, alkenes,...Ch. 11.5 - Give the IUPAC name for each of the following: a....Ch. 11.5 - Give the IUPAC name for each of the following: a....Ch. 11.5 - Draw the condensed structural formula, or...Ch. 11.5 - Prob. 11.28PPCh. 11.6 - Give the IUPAC name for each of the following,...Ch. 11.6 - Give the IUPAC name for each of the following,...Ch. 11.6 - Draw the condensed structural formula for each of...Ch. 11.6 - Prob. 11.32PPCh. 11.7 - Draw the structural formula for the product in...Ch. 11.7 - Draw the structural formula for the product in...Ch. 11.8 - Give the IUPAC name for each of the following: a....Ch. 11.8 - Give the IUPAC name for each of the following: a....Ch. 11.8 - Draw the line-angle formula for each of the...Ch. 11.8 - Draw the line-angle formula for each of the...Ch. 11.8 - Write the balanced chemical equation for the...Ch. 11.8 - Write the balanced chemical equation for the...Ch. 11 - Prob. 11.41UTCCh. 11 - Prob. 11.42UTCCh. 11 - Prob. 11.43UTCCh. 11 - Prob. 11.44UTCCh. 11 - Convert each of the following line-angle formulas...Ch. 11 - Convert each of the following line-angle formulas...Ch. 11 - Give the IUPAC name for each of the following:...Ch. 11 - Give the IUPAC name for each of the following:...Ch. 11 - Give the IUPAC name (including cis or trans, if...Ch. 11 - Give the LUPAC name (including cis or trans, if...Ch. 11 - Prob. 11.51APPCh. 11 - Prob. 11.52APPCh. 11 - Name each of the following aromatic compounds:...Ch. 11 - Prob. 11.54APPCh. 11 - Draw the condensed structural or line-angle...Ch. 11 - Draw the condensed structural or line-angle...Ch. 11 - Draw the cis and trans isomers for each of the...Ch. 11 - Draw the cis and trans isomers for each of the...Ch. 11 - Prob. 11.59APPCh. 11 - Draw the line-angle formula for each of the...Ch. 11 - Write a balanced chemical equation for the...Ch. 11 - Write a balanced chemical equation for the...Ch. 11 - Give the name for the product from the...Ch. 11 - Give the name for the product from the...Ch. 11 - Draw the condensed structural or line-angle...Ch. 11 - Draw the condensed structural or line-angle...Ch. 11 - Prob. 11.67CPCh. 11 - Prob. 11.68CPCh. 11 - Prob. 11.69CPCh. 11 - Prob. 11.70CPCh. 11 - Prob. 11.71CPCh. 11 - Prob. 11.72CPCh. 11 - Prob. 11.73CPCh. 11 - Margarines are produced from the hydrogenation of...
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- 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-CH3arrow_forwardd. CH3-CH2-C-OH 16.58 Which of the following compounds are soluble in water? (16.2, 16.5) а. СH3 — СН, — СH, —С-ОН b. CH3-C-0-CH3 ers c. CH3-CH2-CH2- ОН acid Su d. .1, 16.59 Draw the condensed structural formulas for the products from each of the following reactions: (16.2, 16.3) daim a. CH3-CH2-C-OH + H,O A b. CH3-CH,-C-OH + KOH ОН c acid H, heat с. acid "ОН + С—ОН H*, heat + HO–CH2 CH3 2 d. 16.60 Draw the condensed structural formulas for the products from each of the following reactions: (16.2, 16.3) olone odw a. CH3-C -OH + NaOH || b. CHз— С— ОН + Н2О с. ОН + КОН O=arrow_forward(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 CH3CH₂CH₂CH₂CH₂CH3arrow_forward
- What is the IUPAC name of the following compounds?arrow_forward(10, 6) Draw structural formulas for all of the enol forms of the carbonyl compounds below. You do not have to consider stereochemistry. Consider stereoisomeric enols as a single enol form. In the case of dicarbonyl compounds, do not include stuctures in which both carbonyl groups are present as enols.arrow_forward11.36 Give the IUPAC name for each of the following: a. b. C. Br CI Br CI OH CI CIarrow_forward
- Aa.45.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_forward7. Draw a Fischer projection of each enantiomer of the compound shown below. Then label each enantiomer with its relative configuration. (5.17e). HO OH Harrow_forward
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