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HOMEWORK ON CHAPTER 5 1. Define the following terms: a. Diastereomers b. Enantiomers c. Meso compound d. Optically active compound e. Racemic mixture f. Chiral molecule g. Plane of symmetry 2. The observed rotation for 100 mL of an aqueous solution containing 1g of sucrose, placed in a 2-decimeter sample tube, is +1.33° at 25°C (using sodium lamp). Calculate the specific rotation of sucrose 3. Draw the formula of an unsaturated bromide, C5H9Br, that can show: a. Neither cis-trans isomerism nor optical activity b. Cis-trans isomerism but no optical activity c. No cis-trans isomerism but optical activity d. Cis-trans isomerism and optical activity 4. What can you say about the stereochemistry of the products in the following reactions: Ht H20 CHCH CH=CHt H CH, CH-CHCH b. снснсн - СH OH H;o + OH Ott

HOMEWORK ON CHAPTER 5 1. Define the following terms: a. Diastereomers b. Enantiomers c. Meso compound d. Optically active compound e. Racemic mixture f. Chiral molecule g. Plane of symmetry 2. The observed rotation for 100 mL of an aqueous solution containing 1g of sucrose, placed in a 2-decimeter sample tube, is +1.33° at 25°C (using sodium lamp). Calculate the specific rotation of sucrose 3. Draw the formula of an unsaturated bromide, C5H9Br, that can show: a. Neither cis-trans isomerism nor optical activity b. Cis-trans isomerism but no optical activity c. No cis-trans isomerism but optical activity d. Cis-trans isomerism and optical activity 4. What can you say about the stereochemistry of the products in the following reactions: Ht H20 CHCH CH=CHt H CH, CH-CHCH b. снснсн - СH OH H;o + OH Ott

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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HOMEWORK ON CHAPTER 5 1. Define the following terms: a. Diastereomers b. Enantiomers c. Meso compound d. Optically active compound e. Racemic mixture f. Chiral molecule g. Plane of symmetry 2. The observed rotation for 100 mL of an aqueous solution containing 1g of sucrose, placed in a 2-decimeter sample tube, is +1.33° at 25°C (using sodium lamp). Calculate the specific rotation of sucrose 3. Draw the formula of an unsaturated bromide, C5H9Br, that can show: a. Neither cis-trans isomerism nor optical activity b. Cis-trans isomerism but no optical activity c. No cis-trans isomerism but optical activity d. Cis-trans isomerism and optical activity 4. What can you say about the stereochemistry of the products in the following reactions: Ht H20 CHCH CH=CHt H CH, CH-CHCH b. снснсн - СH OH H;o + OH Ott
Transcribed Image Text:HOMEWORK ON CHAPTER 5 1. Define the following terms: a. Diastereomers b. Enantiomers c. Meso compound d. Optically active compound e. Racemic mixture f. Chiral molecule g. Plane of symmetry 2. The observed rotation for 100 mL of an aqueous solution containing 1g of sucrose, placed in a 2-decimeter sample tube, is +1.33° at 25°C (using sodium lamp). Calculate the specific rotation of sucrose 3. Draw the formula of an unsaturated bromide, C5H9Br, that can show: a. Neither cis-trans isomerism nor optical activity b. Cis-trans isomerism but no optical activity c. No cis-trans isomerism but optical activity d. Cis-trans isomerism and optical activity 4. What can you say about the stereochemistry of the products in the following reactions: Ht H20 CHCH CH=CHt H CH, CH-CHCH b. снснсн - СH OH H;o + OH Ott
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