Chemistry & Chemical Reactivity
Chemistry & Chemical Reactivity
9th Edition
ISBN: 9781133949640
Author: John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher: Cengage Learning
Question
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Chapter 23, Problem 108SCQ
Interpretation Introduction

Interpretation:

The reason for why there is a high barrier to rotation arround a carbon–carbon double bond than carbon–carbon single bond has to be explained

Concept introduction:

In Orbital overlap model of bonding , two nuclei’s of two atoms are approach each other and overlap their atomic orbitals. As the overlapping the energy increases, the interaction decreases.

After some distance the minimum energy is reached and it corresponds to the bonding distance. The two atoms of nuclei begin to repel and energy increases.

There is a high barrier to rotation arround a carbon –carbon double bond than carbon-carbon single bond because higher energy require to break the pi-bond than the sigma bond.

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(11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B Bond A Bond C a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. Weakest Bond Strongest Bond b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. c. (5pts) Use principles discussed in lecture, supported by relevant structures, to succinctly explain the why your part b (i) radical is more stable than your part b(ii) radical. Written explanation can be no more than one-two succinct sentence(s)!

Chapter 23 Solutions

Chemistry & Chemical Reactivity

Ch. 23.3 - Draw the structure of 1-butanol and alcohols that...Ch. 23.3 - Prob. 1RCCh. 23.3 - Prob. 2RCCh. 23.3 - What is the hybridization of nitrogen in...Ch. 23.3 - Prob. 4RCCh. 23.4 - (a) Name each of the following compounds and its...Ch. 23.4 - Prob. 1RCCh. 23.4 - Prob. 2RCCh. 23.4 - Prob. 3RCCh. 23.4 - Prob. 4RCCh. 23.4 - Prob. 1QCh. 23.4 - Prob. 2QCh. 23.4 - Prob. 3QCh. 23.5 - Kevlar is a well-known polymer that is now used to...Ch. 23.5 - Prob. 1QCh. 23.5 - Prob. 2QCh. 23.5 - Prob. 3QCh. 23.5 - Prob. 1RCCh. 23.5 - What is the atom economy for the reaction of...Ch. 23.5 - Prob. 5QCh. 23.5 - If drinking from a polycarbonate bottle, does a 15...Ch. 23.5 - Assume you weigh 156 lb. How much BPA do you...Ch. 23.5 - Prob. 8QCh. 23 - Prob. 1PSCh. 23 - What is the molecular formula for an alkane with...Ch. 23 - Prob. 3PSCh. 23 - Prob. 4PSCh. 23 - One of the structural isomers with the formula...Ch. 23 - Prob. 6PSCh. 23 - Prob. 7PSCh. 23 - Give the systematic name for the following alkane....Ch. 23 - Draw the structure of each of the following...Ch. 23 - Draw structures for the following compounds. (a)...Ch. 23 - Prob. 11PSCh. 23 - Prob. 12PSCh. 23 - Draw the structure of the chair form of...Ch. 23 - Prob. 14PSCh. 23 - Prob. 15PSCh. 23 - Prob. 16PSCh. 23 - Prob. 17PSCh. 23 - Prob. 18PSCh. 23 - Prob. 19PSCh. 23 - What structural requirement is necessary for an...Ch. 23 - A hydrocarbon with the formula C5H10, can be...Ch. 23 - Prob. 22PSCh. 23 - Prob. 23PSCh. 23 - Prob. 24PSCh. 23 - The compound 2-bromobutane is a product of...Ch. 23 - The compound 2,3-dibromo-2-methylhexane is formed...Ch. 23 - Prob. 27PSCh. 23 - Prob. 28PSCh. 23 - Prob. 29PSCh. 23 - Prob. 30PSCh. 23 - Prob. 31PSCh. 23 - Give the systematic name for each of the following...Ch. 23 - Prob. 33PSCh. 23 - Write an equation for the preparation of...Ch. 23 - Prob. 35PSCh. 23 - Prob. 36PSCh. 23 - Prob. 37PSCh. 23 - Prob. 38PSCh. 23 - Prob. 39PSCh. 23 - Name the following amines: (a) CH3CH2CH2NH2 (b)...Ch. 23 - Draw structural formulas for the four possible...Ch. 23 - Prob. 42PSCh. 23 - Prob. 43PSCh. 23 - Prob. 44PSCh. 23 - Prob. 45PSCh. 23 - Prob. 46PSCh. 23 - Prob. 47PSCh. 23 - Prob. 48PSCh. 23 - Prob. 49PSCh. 23 - Prob. 50PSCh. 23 - Give the structural formula and systematic name...Ch. 23 - Prob. 52PSCh. 23 - Prob. 53PSCh. 23 - Prob. 54PSCh. 23 - Prob. 55PSCh. 23 - Prob. 56PSCh. 23 - Prob. 57PSCh. 23 - Prob. 58PSCh. 23 - Prob. 59PSCh. 23 - Prob. 60PSCh. 23 - Identify the functional groups in the following...Ch. 23 - Prob. 62PSCh. 23 - Prob. 63PSCh. 23 - Prob. 64PSCh. 23 - Prob. 65PSCh. 23 - Prob. 66PSCh. 23 - Prob. 67GQCh. 23 - Prob. 68GQCh. 23 - Prob. 69GQCh. 23 - Prob. 70GQCh. 23 - Prob. 71GQCh. 23 - Prob. 72GQCh. 23 - Prob. 73GQCh. 23 - Write equations for the following reactions,...Ch. 23 - Prob. 75GQCh. 23 - Prob. 76GQCh. 23 - Draw the structure of each of the following...Ch. 23 - Prob. 78GQCh. 23 - Prob. 79GQCh. 23 - Draw structural formulas for possible isomers with...Ch. 23 - Prob. 81GQCh. 23 - Prob. 82GQCh. 23 - Prob. 83GQCh. 23 - Prob. 84GQCh. 23 - Prob. 85GQCh. 23 - Prob. 86GQCh. 23 - Draw the structure of glyceryl trilaurate, a fat....Ch. 23 - Prob. 88GQCh. 23 - Prob. 89GQCh. 23 - Prob. 90GQCh. 23 - Prob. 91GQCh. 23 - There are three ethers with the formula C4H10O....Ch. 23 - Review the opening photograph about chocolate...Ch. 23 - Prob. 94GQCh. 23 - Prob. 95ILCh. 23 - Prob. 96ILCh. 23 - Prob. 97ILCh. 23 - Prob. 98ILCh. 23 - Prob. 99ILCh. 23 - Prob. 100ILCh. 23 - Prob. 101ILCh. 23 - Prob. 102ILCh. 23 - Prob. 103ILCh. 23 - Prob. 104ILCh. 23 - Prob. 105ILCh. 23 - Prob. 106ILCh. 23 - Prob. 107SCQCh. 23 - Prob. 108SCQCh. 23 - Prob. 109SCQCh. 23 - Prob. 110SCQCh. 23 - Prob. 111SCQCh. 23 - Prob. 112SCQCh. 23 - Prob. 113SCQ
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