Connect 1-Semester Access Card for General, Organic, & Biological Chemistry
3rd Edition
ISBN: 9781259815072
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
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Question
Chapter 13, Problem 13.93P
Interpretation Introduction
(a)
Interpretation:
The two constitutional isomers formed when linoleic acid is partially hydrogenated with one equivalent of H2 need to be identified.
Concept Introduction:
- Fatty acids are carboxylic acids consisting of a long hydrocarbon chain with a terminal
carboxylic acid group. - The hydrocarbon chain can be saturated (saturated fatty acids) or unsaturated (unsaturated fatty acids)
- Hydrogenation refers to the process in which hydrogen is added across a carbon-carbon double bond associated with unsaturated fatty acids.
Interpretation Introduction
(b)
Interpretation:
The product when linoleic acid is completely hydrogenated by H2 needs to be identified.
Concept Introduction:
- Fatty acids are carboxylic acids consisting of a long hydrocarbon chain with a terminal carboxylic acid group.
- The hydrocarbon chain can be saturated (saturated fatty acids) or unsaturated (unsaturated fatty acids)
- Hydrogenation refers to the process in which hydrogen is added across a carbon-carbon double bond associated with unsaturated fatty acids.
Interpretation Introduction
(c)
Interpretation:
The product formed during the hydrogenation of linoleic acid when one of the cis double bonds is converted to a trans double bond needs to be identified.
Concept Introduction:
- Fatty acids are carboxylic acids consisting of a long hydrocarbon chain with a terminal carboxylic acid group.
- The hydrocarbon chain can be saturated (saturated fatty acids) or unsaturated (unsaturated fatty acids)
- Hydrogenation refers to the process in which hydrogen is added across a carbon-carbon double bond associated with unsaturated fatty acids.
- Cis-trans isomers are geometric isomers. Cis isomers are isomers where functional groups appear on the same side of a double bond; in trans isomers, they appear on opposite sides of a double bond.
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Chapter 13 Solutions
Connect 1-Semester Access Card for General, Organic, & Biological Chemistry
Ch. 13.1 - Convert each condensed structure to a complete...Ch. 13.1 - Prob. 13.2PCh. 13.1 - Complete the structure of zingiberene, a component...Ch. 13.2 - Prob. 13.4PCh. 13.2 - Prob. 13.5PCh. 13.2 - Prob. 13.6PCh. 13.3 - Prob. 13.7PCh. 13.3 - Prob. 13.8PCh. 13.3 - Prob. 13.9PCh. 13.3 - Prob. 13.10P
Ch. 13.3 - Prob. 13.11PCh. 13.3 - Prob. 13.12PCh. 13.3 - Prob. 13.13PCh. 13.4 - Prob. 13.14PCh. 13.6 - Prob. 13.15PCh. 13.6 - Prob. 13.16PCh. 13.6 - Prob. 13.17PCh. 13.6 - Prob. 13.18PCh. 13.6 - Prob. 13.19PCh. 13.7 - Prob. 13.20PCh. 13.8 - Prob. 13.21PCh. 13.8 - Prob. 13.22PCh. 13.10 - Give the IUPAC name of each compound.
Ch. 13.10 - Prob. 13.24PCh. 13.11 - Prob. 13.25PCh. 13.12 - Prob. 13.26PCh. 13.13 - Prob. 13.27PCh. 13.13 - Prob. 13.28PCh. 13 - Anethole, the major constituent of anise oil, is...Ch. 13 - Prob. 13.30PCh. 13 - What is the molecular formula for a hydrocarbon...Ch. 13 - Prob. 13.32PCh. 13 - Prob. 13.33PCh. 13 - Prob. 13.34PCh. 13 - Prob. 13.35PCh. 13 - Prob. 13.36PCh. 13 - Give the IUPAC name for each molecule depicted in...Ch. 13 - Give the IUPAC name for each molecule depicted in...Ch. 13 - Give the IUPAC name for each compound. a....Ch. 13 - Give the IUPAC name for each compound. d....Ch. 13 - Prob. 13.41PCh. 13 - Prob. 13.42PCh. 13 - Give the structure corresponding to each IUPAC...Ch. 13 - Prob. 13.44PCh. 13 - Each of the following IUPAC names is incorrect....Ch. 13 - Each of the following IUPAC names is incorrect....Ch. 13 - Prob. 13.47PCh. 13 - Prob. 13.48PCh. 13 - Prob. 13.49PCh. 13 - Label the carbon-carbon double bond as cis or...Ch. 13 - Prob. 13.51PCh. 13 - Prob. 13.52PCh. 13 - Prob. 13.53PCh. 13 - Prob. 13.54PCh. 13 - Prob. 13.55PCh. 13 - Prob. 13.56PCh. 13 - Prob. 13.57PCh. 13 - Prob. 13.58PCh. 13 - Prob. 13.59PCh. 13 - Prob. 13.60PCh. 13 - What alkyd halide is formed when each alkene is...Ch. 13 - Prob. 13.62PCh. 13 - Prob. 13.63PCh. 13 - Prob. 13.64PCh. 13 - What alkene is needed as a starting material to...Ch. 13 - Prob. 13.66PCh. 13 - Prob. 13.67PCh. 13 - Prob. 13.68PCh. 13 - Prob. 13.69PCh. 13 - Prob. 13.70PCh. 13 - Prob. 13.71PCh. 13 - Prob. 13.72PCh. 13 - Prob. 13.73PCh. 13 - Prob. 13.74PCh. 13 - Prob. 13.75PCh. 13 - Prob. 13.76PCh. 13 - Prob. 13.77PCh. 13 - Prob. 13.78PCh. 13 - Prob. 13.79PCh. 13 - Prob. 13.80PCh. 13 - Prob. 13.81PCh. 13 - Are o-bromochlorobenzene and m-bromochlorobenzene...Ch. 13 - Give the structure corresponding to each IUPAC...Ch. 13 - Give the structure corresponding to each IUPAC...Ch. 13 - Prob. 13.85PCh. 13 - Prob. 13.86PCh. 13 - Prob. 13.87PCh. 13 - Prob. 13.88PCh. 13 - Prob. 13.89PCh. 13 - Prob. 13.90PCh. 13 - Prob. 13.91PCh. 13 - Prob. 13.92PCh. 13 - Prob. 13.93PCh. 13 - Eleostearic acid is an unsaturated fatty acid...Ch. 13 - Prob. 13.95PCh. 13 - Prob. 13.96PCh. 13 - Prob. 13.97PCh. 13 - Prob. 13.98PCh. 13 - Prob. 13.99PCh. 13 - Prob. 13.100PCh. 13 - Prob. 13.101PCh. 13 - Prob. 13.102PCh. 13 - Answer the following questions about compound A,...Ch. 13 - Prob. 13.104PCh. 13 - Prob. 13.105PCh. 13 - Prob. 13.106PCh. 13 - Prob. 13.107CPCh. 13 - Prob. 13.108CP
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