Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
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Textbook Question
Chapter 5, Problem 21PP
Practice Problem 5.21
The following are formulas for three compounds, written in noneclipsed conformations. In each instance tell which compound (A, 8, or C on the previous page) each formula represents.
(a)
(b)
(c)
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2.35 Consider 1-bromo-2-methylpropane and draw the following.(a) The staggered conformation(s) of lowest energy(b) The staggered conformation(s) of highest energy
2.34 Consider 1-bromopropane, CH3CH2CH2Br.(a) Draw a Newman projection for the conformation in which !CH3 and !Br are anti (dihedral angle 1808).(b) Draw Newman projections for the conformations in which !CH3 and !Br are gauche (dihedral angles 608 and 3008).(c) Which of these is the lowest energy conformation?(d) Which of these conformations, if any, are related by reflection?
(a) which if the structure of trans-1,2-dimethylcyclopentane?
(b) which is the most stable conformation of 1-bromo-2-ethylcyclohexane?
(c) which is the least stable conformation of 1-bromo-2-ethylcyclohexane?
(d) which is the more stable configuration of 1,3-dimethylcyclopentane?
*Et = ethyl
Chapter 5 Solutions
Organic Chemistry
Ch. 5 - Prob. 1PPCh. 5 - Prob. 2PPCh. 5 - Prob. 3PPCh. 5 - Prob. 4PPCh. 5 - Prob. 5PPCh. 5 - Prob. 6PPCh. 5 - Prob. 7PPCh. 5 - Practice Problem 5.8 Write three-dimensional...Ch. 5 - Prob. 9PPCh. 5 - Prob. 10PP
Ch. 5 - Practice Problem 5.11 List the substituents in...Ch. 5 - Prob. 12PPCh. 5 - Practice Problem 5.13 Tell whether the two...Ch. 5 - Prob. 14PPCh. 5 - Prob. 15PPCh. 5 - Prob. 16PPCh. 5 - Prob. 17PPCh. 5 - Prob. 18PPCh. 5 - Prob. 19PPCh. 5 - Prob. 20PPCh. 5 - Practice Problem 5.21 The following are formulas...Ch. 5 - Practice Problem 5.22 Write three-dimensional...Ch. 5 - Prob. 23PPCh. 5 - Practice Problem 5.24 Give names chat include (R)...Ch. 5 - Prob. 25PPCh. 5 - Prob. 26PPCh. 5 - Prob. 27PPCh. 5 - Prob. 28PPCh. 5 - Practice Problem 5.29 Write formulas for all of...Ch. 5 - Prob. 30PPCh. 5 - Prob. 31PPCh. 5 - Prob. 32PPCh. 5 - Prob. 33PCh. 5 - Prob. 34PCh. 5 - 5.35 Designate the (R) or (S) configuration at...Ch. 5 - Prob. 36PCh. 5 - (a) Write the structure of...Ch. 5 - Shown below are Newman projection formulas for...Ch. 5 - 5.39 Write appropriate structural formulas...Ch. 5 - Discuss whether each of the following compounds...Ch. 5 - Prob. 42PCh. 5 - Prob. 43PCh. 5 - Compound F has the molecular formula C5H8 and is...Ch. 5 - Prob. 45PCh. 5 - Prob. 46PCh. 5 - Prob. 47PCh. 5 - For the following molecule, draw its enantiomer as...Ch. 5 - 5.49 (Use models to solve this...Ch. 5 - 5.50 (Use models to solve this...Ch. 5 - (Use models co solve this problem.) Write...Ch. 5 - 5.52 Tartaric acid was an important compound in...Ch. 5 - Prob. 53PCh. 5 - Prob. 54PCh. 5 - Prob. 55PCh. 5 - Prob. 1LGPCh. 5 - Prob. 2LGPCh. 5 - Prob. 3LGP
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- Draw the two chair conformations of the following substituted cyclohexanes. In each case, label the more stable conformation.(a) trans-1,2-diethylcyclohexanearrow_forwardConsider 1-bromopropane, CH3CH2CH2Br. (a) Draw a Newman projection for the conformation in which CH3 and -Br are anti (dihedral angle 180°). (b) Draw Newman projections for the conformations in which - CH3 and -Br are gauche (dihedral angles 60° and 300°). (c) Which of these is the lowest energy conformation? (d) Which of these conformations, if any, are related by reflection?arrow_forward2.35 Write a structural formula for each of the following compounds: (a) 6-Isopropyl-2,3-dimethylnonane (b) 4-tert-Butyl-3-methylheptane (c) 4-Isobutyl-1,1-dimethylcyclohexane (d) sec-Butylcycloheptane (e) Cyclobutylcyclopentanearrow_forward
- 3. (20) Cyclohexane may go through ring-flipping as shown below. 5 (a) Draw both of the possible chair conformations for cis-1-tert-butyl-4-methylcyclohexane by copying the scheme above followed by adding appropriate substituents to axial or equatorial positions. (b) Circle the more stable conforms of (A) and (B)arrow_forward5.76 2,3-Dibromoprop-1-ene (C3H4Br₂) has four H atoms. Suppose that any of these H atoms can be replaced by a Cl atom to yield a molecule with the formula C3H3Br₂Cl. (a) Identify two H atoms where this substitution would yield constitutional isomers of C3H3Br₂Cl; (b) enantiomers of C3H3Br₂Cl; (c) diastereomers of C3H3Br₂Cl. co 11 HHH Juods H Brugtrio 2 bas A 2,3-Dil so ontemme A chon Br 2,3-Dibromoprop-1-enearrow_forward(a) All Isomers have the same molecular formulae. Explain this further. Hint what does it mean to have the same molecular formulae? (b) What is Constitutional (structural) isomerism? Hint, isomers are different, so what is different between a pair of constitutional isomers (see the chart on the last page for examples). (c) What is Conformational isomerism?arrow_forward
- Please answer D, E, Farrow_forwardcan i see the answers on section 4.41 D, F, G In the Organic Chemistry: Principles And Mechanisms (second Edition) 2nd Editionarrow_forwardWrite the two chair conformations of each of the following and in each part designate whichconformation would be the more stable: (a) cis-1-tert-butyl-3-methylcyclohexane, (b) trans-1-tert-butyl-3-methylcyclohexane, (c) trans-1-tert-butyl-4-methylcyclohexane, ( d) cis-1-tert-butyl-4-methylcyclohexane.arrow_forward
- 3B. For each compound below, draw two chair conformations. Indicate whether the substituents are axial or equatorial. Indicate which chair conformation is more stable. (you need to draw conformations of the exact molecule, not its mirror image or diastereomer) (a) (b) (c) Ме Me Et "Et Et Mearrow_forwardConsider 1-bromopropane, CH3CH2CH2Br. (a) Which of these is the lowest energy conformation?arrow_forwardDraw the more stable chair conformation for each of the following disubstituted cyclohexanes. (a) OH (b) OH (c) (d) (e) (f) „CBr3 CBr3 "Cl3 CCI3 Cl3arrow_forward
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