Organic Chemistry
6th Edition
ISBN: 9781936221349
Author: Marc Loudon, Jim Parise
Publisher: W. H. Freeman
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Chapter 19, Problem 19.17P
Interpretation Introduction
Interpretation:
The carbonyl compound which forms the greater proportion of cyanohydrin at equilibrium is to be identified. The structure of the cyanohydrin is to be drawn. The reason for the same is to be explained.
Concept introduction:
The delocalization of electrons results in the formation of resonance structure. The curved-arrow notation traces the flow of the electrons in a compound. This notation is used to derive the resonance structure.
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What is the name of this compound?
O Phenoxy-2-ethylbutanoic acid
O2-ethylbutyl benzoate
O benzyl 2-ethylbutanoate
Phenyl 2-isopropylbutanoate
O Phenyl 2-ethylbutanoate
What explains why many aldehydes and ketones can undergo self- condensation reactions in basic conditions?
The alpha carbon can lose a proton and act like a nucleophile and the carbonyl carbon a an electrophile
O The alpha carbon can gain a proton and act like an electrophile and the carbonyl carbon is a nucleophile
O The oxygen of the carbonyl group can attack the carbon of the carbonyl group
Only esters can undergo self-condensation reactions
Name the following organic compound:
CH₂
CH₂
H3C
CH₂
OH
O 2-oxo-5-pentanol
O 4-oxo-1-pentanol
O 5-hydroxy-2-pentanone
O hydroxypentanone
O 1-hydroxy-4-pentanone
Chapter 19 Solutions
Organic Chemistry
Ch. 19 - Prob. 19.1PCh. 19 - Prob. 19.2PCh. 19 - Prob. 19.3PCh. 19 - Prob. 19.4PCh. 19 - Prob. 19.5PCh. 19 - Prob. 19.6PCh. 19 - Prob. 19.7PCh. 19 - Prob. 19.8PCh. 19 - Prob. 19.9PCh. 19 - Prob. 19.10P
Ch. 19 - Prob. 19.11PCh. 19 - Prob. 19.12PCh. 19 - Prob. 19.13PCh. 19 - Prob. 19.14PCh. 19 - Prob. 19.15PCh. 19 - Prob. 19.16PCh. 19 - Prob. 19.17PCh. 19 - Prob. 19.18PCh. 19 - Prob. 19.19PCh. 19 - Prob. 19.20PCh. 19 - Prob. 19.21PCh. 19 - Prob. 19.22PCh. 19 - Prob. 19.23PCh. 19 - Prob. 19.24PCh. 19 - Prob. 19.25PCh. 19 - Prob. 19.26PCh. 19 - Prob. 19.27PCh. 19 - Prob. 19.28PCh. 19 - Prob. 19.29PCh. 19 - Prob. 19.30PCh. 19 - Prob. 19.31PCh. 19 - Prob. 19.32PCh. 19 - Prob. 19.33PCh. 19 - Prob. 19.34PCh. 19 - Prob. 19.35PCh. 19 - Prob. 19.36PCh. 19 - Prob. 19.37PCh. 19 - Prob. 19.38PCh. 19 - Prob. 19.39PCh. 19 - Prob. 19.40APCh. 19 - Prob. 19.41APCh. 19 - Prob. 19.42APCh. 19 - Prob. 19.43APCh. 19 - Prob. 19.44APCh. 19 - Prob. 19.45APCh. 19 - Prob. 19.46APCh. 19 - Prob. 19.47APCh. 19 - Prob. 19.48APCh. 19 - Prob. 19.49APCh. 19 - Prob. 19.50APCh. 19 - Prob. 19.51APCh. 19 - Prob. 19.53APCh. 19 - Prob. 19.54APCh. 19 - Prob. 19.55APCh. 19 - Prob. 19.56APCh. 19 - Prob. 19.57APCh. 19 - Prob. 19.58APCh. 19 - Prob. 19.59APCh. 19 - Prob. 19.60APCh. 19 - Prob. 19.61APCh. 19 - Prob. 19.62APCh. 19 - Prob. 19.63APCh. 19 - Prob. 19.64APCh. 19 - Prob. 19.65APCh. 19 - Prob. 19.66APCh. 19 - Prob. 19.67APCh. 19 - Prob. 19.68APCh. 19 - Prob. 19.69APCh. 19 - Prob. 19.70APCh. 19 - Prob. 19.71APCh. 19 - Prob. 19.72AP
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- Hydration of aldehydes and ketones can be catalyzed by acid or base. Bases catalyze hydration by: protonating the carbonyl oxygen making the carbonyl group more electrophilic employing hydroxide ion, which is a better nucleophile than water making the carbonyl group less electrophilic shifting the equilibrium position of the reaction to favor productsarrow_forward1-Octen-3-ol is a potent mosquito attractant commonly used in mosquito traps. A number of reactions, including hydrogenation, will transform 1-octen-3-ol into a less effective molecule. Draw the structure of a hydrogenation product of 1-octen-3-ol.arrow_forward19) What is the IUPAC name for this compound? CH3 H3C- -сн—сH,—CH2--с— он O 2-methyl-4-butanoic acid pentanoic acid 2-methyl butyric acid 3-methylbutanoic acid O 2-methylbutanoic acidarrow_forward
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