Consider the following organic reaction, in which one halogen replaces another in an | StudySoup

Textbook Solutions for Chemistry: The Molecular Nature of Matter and Change - Standalone book

Chapter 16 Problem 16.118

Question

Consider the following organic reaction, in which one halogen replaces another in an alkyl halide: CH3CH2Br 1 KI - CH3CH2I 1 KBr In acetone, this particular reaction goes to completion because KI is soluble in acetone but KBr is not. In the mechanism, I2 approaches the carbon opposite to the Br (see Figure 16.20, p. 704, with I2 instead of OH2). After Br2 has been replaced by I 2 and precipitates as KBr, other I2 ions react with the ethyl iodide by the same mechanism. (a) If we designate the carbon bonded to the halogen as C-1, what is the shape around C-1 and the hybridization of C-1 in ethyl iodide? (b) In the transition state, one of the two lobes of the unhybridized 2p orbital of C-1 overlaps a p orbital of I, while the other lobe overlaps a p orbital of Br. What is the shape around C-1 and the hybridization of C-1 in the transition state? (c) The deuterated reactant, CH3CHDBr (where D is deuterium, 2H), has two optical isomers because C-1 is chiral. If the reaction is run with one of the isomers, the ethyl iodide is not optically active. Explain.

Solution

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The first step in solving 16 problem number 118 trying to solve the problem we have to refer to the textbook question: Consider the following organic reaction, in which one halogen replaces another in an alkyl halide: CH3CH2Br 1 KI - CH3CH2I 1 KBr In acetone, this particular reaction goes to completion because KI is soluble in acetone but KBr is not. In the mechanism, I2 approaches the carbon opposite to the Br (see Figure 16.20, p. 704, with I2 instead of OH2). After Br2 has been replaced by I 2 and precipitates as KBr, other I2 ions react with the ethyl iodide by the same mechanism. (a) If we designate the carbon bonded to the halogen as C-1, what is the shape around C-1 and the hybridization of C-1 in ethyl iodide? (b) In the transition state, one of the two lobes of the unhybridized 2p orbital of C-1 overlaps a p orbital of I, while the other lobe overlaps a p orbital of Br. What is the shape around C-1 and the hybridization of C-1 in the transition state? (c) The deuterated reactant, CH3CHDBr (where D is deuterium, 2H), has two optical isomers because C-1 is chiral. If the reaction is run with one of the isomers, the ethyl iodide is not optically active. Explain.
From the textbook chapter Kinetics: Rates and Mechanisms of Chemical Reactions you will find a few key concepts needed to solve this.

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Title Chemistry: The Molecular Nature of Matter and Change - Standalone book 7 
Author Martin Silberberg Dr., Patricia Amateis Professor
ISBN 9780073511177

Consider the following organic reaction, in which one halogen replaces another in an

Chapter 16 textbook questions

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