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Concept explainers
(a)
Interpretation:
The skeletal structure of
Concept Introduction:
Fatty acids are long-chain
Unsaturated fatty acids can be defined as the long-chain fatty acids which have a long hydrocarbon chain with −COOH group. In unsaturated fatty acids, the carbon chain must have at least one double bond.
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Answer to Problem 34P
Explanation of Solution
Given:
Fatty acids are long-chain carboxylic acids, which consist of two parts; long hydrocarbon chains and polar −COOH group. The long hydrocarbon chain consists of carbon and H atoms, so it has C-C and C-H bonds only, whereas, the polar −COOH group has polar C=O and C-O bonds. The unsaturated fatty acids have cis and trans-double bonds in the hydrocarbon chain.
In the ball-and-stick model, the red ball represents O atom, the black ball represents C atom and the white ball represents H atoms. Thus, the skeletal structure is:
(b)
Interpretation:
The omega-n designation for the
Concept Introduction:
Fatty acids are long-chain carboxylic acid, which may or may not have unsaturation in the molecule. They react with glycerol to form triglycerides. The reaction is called esterification as a carboxylic acid group reacts with the alcoholic group to form an ester group.
Unsaturated fatty acids can be defined as the long-chain fatty acids which have a long hydrocarbon chain with −COOH group. In unsaturated fatty acids, the carbon chain must have at least one double bond.
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Answer to Problem 34P
The
Explanation of Solution
Fatty acids are long-chain carboxylic acids, which consist of two parts; long hydrocarbon chains and polar −COOH group. If there is at least one double bond in the long hydrocarbon chain of the fatty acid, it is said to be an unsaturated fatty acid.
The unsaturated fatty acids can also classify as omega-n acids. Here, 'n' represents the position of the first
In the given fatty acid
(c)
Interpretation:
The stereoisomer of the
Concept Introduction:
Fatty acids are long-chain carboxylic acid, which may or may not have unsaturation in the molecule. They react with glycerol to form triglycerides. The reaction is called esterification as a carboxylic acid group reacts with the alcoholic group to form an ester group.
Unsaturated fatty acids can be defined as the long-chain fatty acids which have a long hydrocarbon chain with −COOH group. In unsaturated fatty acids, the carbon chain must have at least one double bond.
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Answer to Problem 34P
The stereoisomer of cis-fatty acid must be trans-isomer as given below;
Explanation of Solution
Fatty acids are long-chain carboxylic acids, which consist of two parts; long hydrocarbon chains and polar −COOH group. The double bond can arrange in two ways, i.e., cis and Trans in the hydrocarbon chain of the fatty acid molecule. Hence, the stereoisomer of cis-fatty acid
(d)
Interpretation:
The structure of wax formed by the reaction of
Concept Introduction:
Fatty acids are long-chain carboxylic acid, which may or may not have unsaturation in the molecule. They react with glycerol to form triglycerides. The reaction is called esterification as a carboxylic acid group reacts with the alcoholic group to form an ester group.
Unsaturated fatty acids can be defined as the long-chain fatty acids which have a long hydrocarbon chain with −COOH group. In unsaturated fatty acids, the carbon chain must have at least one double bond.
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Answer to Problem 34P
The skeleton formula of wax formed by the reaction of
Explanation of Solution
Fatty acids are long-chain carboxylic acids, which consist of two parts; long hydrocarbon chains and polar −COOH group. Waxes are a good example of hydrolyzable lipids, which are composed of fatty acid and higher alcohols. They have an ester
Hence, the reaction of
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Chapter 19 Solutions
General, Organic, and Biological Chemistry - 4th edition
- How would you distinguish the following compounds from each other using IR only (GRADED)? NH2 HN VS کر A B VS N. Carrow_forwardQ4: Draw the mirror image of the following molecules. Are the molecules chiral? C/ F CI CI CH3 CI CH3 CI CH3 CH 3 |||||... CH3arrow_forwardQ6: Monochlorination of methylcyclopentane can result in several products. When the chlorination occurs at the C2 position, how many stereoisomers are formed? If more than one is formed, are they generated in equal or unequal amounts? 2arrow_forward
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- Please correct answer and don't use hand ratingarrow_forwardwhen a 0.150 g sample of the compound was burned, it produced 0.138 g CO2 & 0.0566 g H2O. All the nitrogen in a different 0.200 g sample of the compound was converted to NH3, which was found to weigh 0.0238 g. Finally, the chlorine in a 0.125 g sample of the compound was converted to Cl- and by reacting it with AgNO3, all of the chlorine was recovered as the solid AgCl. The AgCl, when dried was found to weigh 0.251 g. What is the empirical formulaarrow_forwardPlease correct answer and don't use hand rating and don't use Ai solutionarrow_forward
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