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OWLv2 for Bettelheim/Brown/Campbell/Farrell/Torres' Introduction to General, Organic and Biochemistry, 11th Edition, [Instant Access], 1 term (6 months)
11th Edition
ISBN: 9781305106734
Author: Frederick A. Bettelheim; William H. Brown; Mary K. Campbell; Shawn O. Farrell; Omar Torres
Publisher: Cengage Learning US
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Question
Chapter 17, Problem 17.45P
Interpretation Introduction
(a)
Interpretation:
The structural formula of keto form for the given enol form should be drawn.
![OWLv2 for Bettelheim/Brown/Campbell/Farrell/Torres' Introduction to General, Organic and Biochemistry, 11th Edition, [Instant Access], 1 term (6 months), Chapter 17, Problem 17.45P , additional homework tip 1](https://content.bartleby.com/tbms-images/9781285869759/Chapter-17/images/html_69759-17-17.45p_1.png)
Concept Introduction:
A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.
![OWLv2 for Bettelheim/Brown/Campbell/Farrell/Torres' Introduction to General, Organic and Biochemistry, 11th Edition, [Instant Access], 1 term (6 months), Chapter 17, Problem 17.45P , additional homework tip 2](https://content.bartleby.com/tbms-images/9781285869759/Chapter-17/images/html_69759-17-17.45p_2.png)
a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.
Interpretation Introduction
(b)
Interpretation:
The structural formula of keto form for the given enol form should be drawn.
![OWLv2 for Bettelheim/Brown/Campbell/Farrell/Torres' Introduction to General, Organic and Biochemistry, 11th Edition, [Instant Access], 1 term (6 months), Chapter 17, Problem 17.45P , additional homework tip 3](https://content.bartleby.com/tbms-images/9781285869759/Chapter-17/images/html_69759-17-17.45p_5.png)
Concept Introduction:
A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.
![OWLv2 for Bettelheim/Brown/Campbell/Farrell/Torres' Introduction to General, Organic and Biochemistry, 11th Edition, [Instant Access], 1 term (6 months), Chapter 17, Problem 17.45P , additional homework tip 4](https://content.bartleby.com/tbms-images/9781285869759/Chapter-17/images/html_69759-17-17.45p_6.png)
a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.
Interpretation Introduction
(c)
Interpretation:
The structural formula of keto form for the given enol form should be drawn.
![OWLv2 for Bettelheim/Brown/Campbell/Farrell/Torres' Introduction to General, Organic and Biochemistry, 11th Edition, [Instant Access], 1 term (6 months), Chapter 17, Problem 17.45P , additional homework tip 5](https://content.bartleby.com/tbms-images/9781285869759/Chapter-17/images/html_69759-17-17.45p_9.png)
Concept Introduction:
A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.
![OWLv2 for Bettelheim/Brown/Campbell/Farrell/Torres' Introduction to General, Organic and Biochemistry, 11th Edition, [Instant Access], 1 term (6 months), Chapter 17, Problem 17.45P , additional homework tip 6](https://content.bartleby.com/tbms-images/9781285869759/Chapter-17/images/html_69759-17-17.45p_10.png)
a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.
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Chapter 17 Solutions
OWLv2 for Bettelheim/Brown/Campbell/Farrell/Torres' Introduction to General, Organic and Biochemistry, 11th Edition, [Instant Access], 1 term (6 months)
Ch. 17.2 - Problem 17-1 Wrtie the IUPAC name for each...Ch. 17.2 - Prob. 17.2PCh. 17.2 - Prob. 17.3PCh. 17.4 - Prob. 17.4PCh. 17.4 - Prob. 17.5PCh. 17.4 - Problem 17-6 Show the reaction of benzaldehyde...Ch. 17.4 - Problem 17-7 Identify all hemiacetals and acetals...Ch. 17.5 - Prob. 17.8PCh. 17 - 17-9 Answer true or false. (a) The one aldehyde...Ch. 17 - Prob. 17.10P
Ch. 17 - 17-11 What is the difference in structure between...Ch. 17 - 17-12 Is it possible for the carbon atom of a...Ch. 17 - 17-13 Which compounds contain carbonyl groups?Ch. 17 - 17-14 Following are structural formulas for two...Ch. 17 - 17-15 Draw structural formulas for the four...Ch. 17 - Prob. 17.16PCh. 17 - Prob. 17.17PCh. 17 - 17-18 Draw structural formulas for these ketones....Ch. 17 - 17-19 Write the JUPAC names for these compounds.Ch. 17 - Prob. 17.20PCh. 17 - 17-2 1 Explain why each name is incorrect. Write...Ch. 17 - Prob. 17.22PCh. 17 - Prob. 17.23PCh. 17 - 17-24 In each pair of compounds, select the one...Ch. 17 - Prob. 17.25PCh. 17 - 17-26 Account for the fact that acetone has a...Ch. 17 - 17-27 Pentane, 1-butanol, and butanal all have...Ch. 17 - 17-28 Show how acetaldehyde can form hydrogen...Ch. 17 - 17-29 Why can’t two molecules of acetone form a...Ch. 17 - 17-30 Answer true or false. (a) The reduction of...Ch. 17 - 17-3 1 Draw a structural formula for the principal...Ch. 17 - Prob. 17.32PCh. 17 - 17-33 What simple chemical test could you use to...Ch. 17 - 17-34 Explain why liquid aldehydes are often...Ch. 17 - 17-35 Suppose that you take a bottle of...Ch. 17 - 17-36 Explain why the reduction of an aldehyde...Ch. 17 - Prob. 17.37PCh. 17 - Prob. 17.38PCh. 17 - Prob. 17.39PCh. 17 - Prob. 17.40PCh. 17 - Prob. 17.41PCh. 17 - Prob. 17.42PCh. 17 - Prob. 17.43PCh. 17 - Prob. 17.44PCh. 17 - Prob. 17.45PCh. 17 - Prob. 17.46PCh. 17 - 17-47 What is the characteristic structural...Ch. 17 - Prob. 17.48PCh. 17 - Prob. 17.49PCh. 17 - Prob. 17.50PCh. 17 - Prob. 17.51PCh. 17 - Prob. 17.52PCh. 17 - Prob. 17.53PCh. 17 - 17-54 Following is the structure of...Ch. 17 - Prob. 17.55PCh. 17 - Prob. 17.56PCh. 17 - Prob. 17.57PCh. 17 - Prob. 17.58PCh. 17 - Prob. 17.59PCh. 17 - 17-60 1-Propanol can be prepared by the reduction...Ch. 17 - Prob. 17.61PCh. 17 - 17-62 Show how to bring about these conversions....Ch. 17 - Prob. 17.63PCh. 17 - Prob. 17.64PCh. 17 - Prob. 17.65PCh. 17 - Prob. 17.66PCh. 17 - 17-67 Draw structural formulas for these...Ch. 17 - Prob. 17.68PCh. 17 - 17-69 Propanal (bp 49°C) and 1-propanol (bp 97°C)...Ch. 17 - 17-70 What simple chemical test could you use to...Ch. 17 - Prob. 17.71PCh. 17 - 17-72 The following molecule is an enediol; each...Ch. 17 - 17-73 Alcohols can be prepared by the...Ch. 17 - 17-74 Glucose, C6H12O6, contains an aldehyde group...Ch. 17 - Prob. 17.75PCh. 17 - Prob. 17.76PCh. 17 - Prob. 17.77PCh. 17 - 17-78 Complete the following equation for these...Ch. 17 - 17-79 Write an equation for each conversion. (a)...
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