Organic Chemistry
11th Edition
ISBN: 9781118133576
Author: T. W. Graham Solomons, Craig Fryhle
Publisher: Wiley, John & Sons, Incorporated
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Chapter 23, Problem 4LGP
Interpretation Introduction
Interpretation:
The structure of phospholipid, all the products which are formed from phospholipid on complete hydrolysis and the products of the given reactions with unsaturated fatty acid moiety of this phospholipid are to be drawn.
Concept Introduction:
▸ Phospholipids are a class of lipids which are a major component of all cell membranes.
▸ The structure of the phospholipid molecule consists of two hydrophobic fatty acids and a hydrophilic phosphate group. The two components are joined together by a glycerol molecule.
▸ Complete hydrolysis of a phospholipid gives two fatty acids (constituting the phospholipid), phosphoric acid and glycerol.
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118.5
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335
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14. Ammonia is produced from the reaction of nitrogen and hydrogen according…
==
Functional Groups
Identifying and drawing hemiacetals and acetals
In the drawing area below, create an acetal with 1 isopropoxy group, 1 hydroxyl group, and a total of 10 carbon atoms.
Explanation
Click and drag to start drawing a
structure.
Check
G
+
State the products (formulas) of the reaction of acetophenone with iodine and NaOH.
Chapter 23 Solutions
Organic Chemistry
Ch. 23 - Prob. 1PPCh. 23 - Prob. 2PPCh. 23 - Prob. 3PPCh. 23 - Prob. 4PPCh. 23 - Prob. 5PPCh. 23 - Prob. 6PPCh. 23 - Prob. 7PPCh. 23 - Prob. 8PPCh. 23 - Prob. 9PPCh. 23 - Prob. 10PP
Ch. 23 - Prob. 11PPCh. 23 - Prob. 12PCh. 23 - 23.15 How would you transform tetradecanal into...Ch. 23 - Prob. 14PCh. 23 - Prob. 15PCh. 23 - When limonene (Section 23.3) is heated strongly,...Ch. 23 - Gadoleic acid (C20H38O2), a fatty acid that can be...Ch. 23 - 23.20 -Phellandrene and -phellandrene are isomeric...Ch. 23 - Prob. 19PCh. 23 - Prob. 20PCh. 23 - Prob. 21PCh. 23 - The initial steps of a laboratory synthesis of...Ch. 23 - Prob. 23PCh. 23 - Prob. 24PCh. 23 - Prob. 25PCh. 23 - 2. The biosynthesis of fatty acids is accomplished...Ch. 23 - Prob. 3LGPCh. 23 - Prob. 4LGPCh. 23 - 23.1 Write an appropriate formula in each box.
Ch. 23 - Give a reagent that would distinguish between each...Ch. 23 - 23.3 What product would be obtained by catalytic...Ch. 23 - Prob. 4QCh. 23 - 23.5 The following compound is a:
(a)...Ch. 23 - Mark off the isoprene units in the previous...Ch. 23 - Prob. 7Q
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- Explanation Check Draw the skeletal ("line") structure of 5-hydroxy-4-methyl-2-pentanone. Click and drag to start drawing a structure. Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Cer ☐ : Carrow_forward1. Using a Model set Build a model for the following compound [CH2BrCI]. 2. Build another model of the mirror image of your first molecule. 3. Place the two models next to each other and take a picture which shows the differences between the two models. 4. Determine the absolute stereochemistry R or S for the two models. 5. Write or type a paragraph to Discuss the stereochemical relationship between the two models of CH2BrCl. You must provide an explanation for your conclusions also provide a description for the colors used to represent each atom in the model's images.arrow_forwardWhat parameters are included in the specific rotation calculation of a pure substance based on measurement from a polarimeter? Select one or more: Density of the sample Pathlength of the sample container Enantiomeric excess of the sample Measured rotation of lightarrow_forward
- V Determine whether the following molecule is a hemiacetal, acetal, or neither and select the appropriate box below. Also, highlight the hemiacetal or acetal carbon if there is one. Explanation O CH O Ohemiacetal Oacetal Oneither Check A 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Cer 000 Ararrow_forward1. Using Online resources and chemical structures hand draw four different organic compounds (not those already shown in your handout) that are chiral, optically active (a pair of enantiomers will count as one). Pay attention to correct stereochemistry 2. Write or type a short paragraph to Discuss the stereochemical relationship between the four compounds.arrow_forward1. Using a Model set Build a model for the following compound [CHBRIF] 2. Build another model of the mirror image of your first molecule. 3. Place the two models next to each other and take a picture which shows the differences between the two models. 4. Determine the absolute stereochemistry R or S for the two models. 5. Write or type a paragraph to Discuss the stereochemical relationship between the two models of CHBгCIF. You must provide an explanation for your conclusions also provide a description for the colors used to representarrow_forward
- The specific rotation of a sample depends upon measured angle of rotation, the density of the sample, and the pathway length of the light. True Falsearrow_forwardConsider the molecule A,B, C and D shown below, (1 x 4) Br NH2 A OH Br 边 H B C D 1. Assign the R/S configuration to each chiral center and identify by circling all the chiral centers. 2. Draw an image for the enantiomer of each of the compounds A, B, C and D.arrow_forwardCould you crystallize one enantiomer of mandelic acid from a racemic mixture (using the typical achiral solvents found in our lab) without preparing a diastereomeric salt? Why or why not? No, because both enantiomers have the same solubility in achiral solvents. than the other. ооо Yes, because one enantiomer has a higher melting point No, because both enantiomers are liquids. Yes, because one enantiomer is more crystalline than the other.arrow_forward
- If the literature value of specific rotation for a chiral compound is -53.6°, what is the enantiomeric excess of a compound with a measured specific rotation of -40.5°?arrow_forwardThe process to determine the configuration, starts by placing the lowest priority substituent toward the back. If the substituents pointing forward decrease in priority in a clockwise order, the configuration is S. If the substituents decrease in priority in a counterclockwise order, the configuration is R. True Falsearrow_forwardIn the drawing area below, create a hemiacetal with 1 hydroxyl group, 1 methoxy group, and a total of 3 carbon atoms. Click and drag to start drawing a structure. Explanation Check Х PO 18 Ar B © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forward
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