Organic Chemistry
6th Edition
ISBN: 9781936221349
Author: Marc Loudon, Jim Parise
Publisher: W. H. Freeman
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Question
Chapter 6, Problem 6.5P
Interpretation Introduction
(a)
Interpretation:
The line-and-wedge representation for the given chiral molecules is to be drawn.
Concept introduction:
The line-and-wedge representation of an organic molecule is the representation in which bonds are represented in three different ways. The bold bond represents the bond that is projecting out of out of the plane. The dash bond represents the bond that is projecting towards the back of the plane. The lines represent the bonds that are in the plane.
Interpretation Introduction
(b)
Interpretation:
The line-and-wedge representation for the given chiral molecules is to be drawn.
Concept introduction:
The line-and-wedge representation of an organic molecule is the representation in which bonds are represented in three different ways. The bold bond represents the bond that is projecting out of the plane. The dash bond represents the bond that is projecting towards the back of the plane. The lines represent the bonds that are in the plane.
Interpretation Introduction
(c)
Interpretation:
The line-and-wedge representation for the given chiral molecules is to be drawn.
Concept introduction:
The line-and-wedge representation of an organic molecule is the representation in which bonds are represented in three different ways. The bold bond represents the bond that is projecting out of the plane. The dash bond represents the bond that is projecting towards the back of the plane. The lines represent the bonds that are in the plane.
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Students have asked these similar questions
1. (a) A widely prescribed antibiotic (1) is shown below. Copy the structure of this compound into your
answer sheet and answer the following questions.
HO.
H.
H2N
(1)
(i) Circle and label five different functional groups present.
(ii) Indicate the geometry (E or Z) of the alkene double bond in the structure. In your answer include
the assignment of priorities.
(iii) Identify ALL the chiral carbons present in compound (1) by placing an asterisk (*) at the
appropriate atoms.
(iv) Select ANY ONE of the chiral centres you have identified in part (iii) above and assign the correct
Cahn-Ingold-Prelog (R, S) configuration. In your answer include the assignment of priorities.
4.(a). Draw the structures of (i) cis-1,4-Dibromocyclohexane and (ii) trans-1,4-
Dibromocyclohexane.
4(b). Draw the most stable conformers of (i) cis-1,4-Dibromocyclohexane and (ii)
trans-1,4-Dibromocyclohexane.
4(c)Which is more stable? (i) cis-1,4-Dibromocyclohexane or (ii) trans-1,4-
Dibromolcyclohexane. Explain the reason for your choice.
If either of the following molecules has a stereogenic carbon (chirality center), give structures for both of the enantiomers.
(a) 2-bromopropane (b) 2-bromobutane
Chapter 6 Solutions
Organic Chemistry
Ch. 6 - Prob. 6.1PCh. 6 - Prob. 6.2PCh. 6 - Prob. 6.3PCh. 6 - Prob. 6.4PCh. 6 - Prob. 6.5PCh. 6 - Prob. 6.6PCh. 6 - Prob. 6.7PCh. 6 - Prob. 6.8PCh. 6 - Prob. 6.9PCh. 6 - Prob. 6.10P
Ch. 6 - Prob. 6.11PCh. 6 - Prob. 6.12PCh. 6 - Prob. 6.13PCh. 6 - Prob. 6.14PCh. 6 - Prob. 6.15PCh. 6 - Prob. 6.16PCh. 6 - Prob. 6.17PCh. 6 - Prob. 6.18PCh. 6 - Prob. 6.19PCh. 6 - Prob. 6.20PCh. 6 - Prob. 6.21PCh. 6 - Prob. 6.22PCh. 6 - Prob. 6.23PCh. 6 - Prob. 6.24PCh. 6 - Prob. 6.25PCh. 6 - Prob. 6.26APCh. 6 - Prob. 6.27APCh. 6 - Prob. 6.28APCh. 6 - Prob. 6.29APCh. 6 - Prob. 6.30APCh. 6 - Prob. 6.31APCh. 6 - Prob. 6.32APCh. 6 - Prob. 6.33APCh. 6 - Prob. 6.34APCh. 6 - Prob. 6.35APCh. 6 - Prob. 6.36APCh. 6 - Prob. 6.37APCh. 6 - Prob. 6.38APCh. 6 - Prob. 6.39APCh. 6 - Prob. 6.40APCh. 6 - Prob. 6.41APCh. 6 - Prob. 6.42APCh. 6 - Prob. 6.43APCh. 6 - Prob. 6.44APCh. 6 - Prob. 6.45APCh. 6 - Prob. 6.46APCh. 6 - Prob. 6.47APCh. 6 - Prob. 6.48APCh. 6 - Prob. 6.49APCh. 6 - Prob. 6.50APCh. 6 - Prob. 6.51APCh. 6 - Prob. 6.52APCh. 6 - Prob. 6.53APCh. 6 - Prob. 6.54AP
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