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.
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.
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.
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.
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
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- Draw the ringed structure for D- Glucosearrow_forwardQuestion 8 (5 marks): A. Draw a structure of saturated fatty acid with 16 carbons (1 mark) and identify its functional groups (1 mark).arrow_forwardWhich of the following types of carbohydrates can be hydrolyzed to give smaller molecules? I. monosaccharides II. disaccharides II. oligosaccharides IV. polysaccharides 7. a.l only b.Il and IV only c. II only d.l and II only e. II, III, and IVarrow_forward
- Which fatty acid would you expect to be have the lowest melting point? # 3 80 F3 71 $ 4 A) CH,CH=CH(CH,), CH=CHCOOH B) CH₂(CH₂),COOH C) CH₂(CH₂),COOH D) CH₂CH=CH(CH₂),COOH E) CH₂(CH₂) ₁4COOH Q F4 dº L % 5 Question 6 of 19 F5 14 <6 F6 & 7 ▷▷ F7 * 0 8 DII F8 9 DD F9 0 7 F10arrow_forward3. Lipids a. What are saturated fats? b. What is the main origin of triacylglycerides or oils? O c. Why do unsaturated oils discolor bromine in solution? d. What functional groups are present in triacylglycerides? and. Why are lipids not soluble in water when they have a polar part? F. What positive function does cholesterol have in the body? pility: Good to go D (Ctrl)arrow_forward1. HO HO OH Monosaccharide 2. Disaccharide H HO Polysaccharide H. OH 3. Starcharrow_forward
- 16. How does a double bond in a fatty acid change the overall structure of the fatty acid? а. The overall structure does not change. b. The more double bonds a fatty acid has, the more linear it is. The more double bonds a fatty acid has, the more flexible it is. d. The more double bonds a fatty acid has, the more bent or kinked it is. С. e. The more double bonds a fatty acid has, the more twisted it is. 17. A polyunsaturated fatty acid contains multiple ketones. carboxylic acids. carbon-carbon double bonds. alcohols. Any of the above ing the deltaarrow_forward12. Monosaccharides are designated with a "D" or "L" in their name. What determines this? A. The bond between a chiral carbon and an OH group in the structure. B. The acyclic monosaccharide contains either a ketone or an aldehyde functional group. C. The molecule has either five or six carbons in its structure. D. The molecule is either cyclic or acyclic. E. The anomeric carbon has an OH group pointing up or down in a drawing of the molecule.arrow_forwardWhich of these fatty acids is considered a "good fat"?arrow_forward
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