ORGANIC CHEMISTRY
5th Edition
ISBN: 9781259977596
Author: SMITH
Publisher: MCG
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Chapter 21, Problem 21.66P
Interpretation Introduction
Interpretation: The structure of the product formed from the given reaction is to be drawn, and an explanation for its formation is to be stated.
Concept introduction: The
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19. Complete the following chart for the incorrect electron configurations shown in the left column.
When drawing the correct electron configuration, assume the same number of electrons that were
shown in the incorrect configuration.
Incorrect Electron
Configuration
2p
↑↓ ↑
2s
↑↓
1s
↑↓↓
ਵੇ ਵੇ ਵੇ
3p
↑
↑
↑
-
38
↑
2p
2s
↑↓
1s
2p
2s
1s
**
↑↓ ↑↓ ↑↑
리리리
Which principle or
rule is violated?
Explain the violated principle
or rule in your own words
Draw the correct
electron configuration
14.36 Draw all reasonable resonance structures for each compound.
a.
+
b.
C.
:O:
d.
:O:
NH2
NH2
:O:
14.32 What diene and dienophile are needed to prepare each compound by a
Diels-Alder reaction?
a.
b.
Chapter 21 Solutions
ORGANIC CHEMISTRY
Ch. 21 - Rank the following compounds in order of...Ch. 21 - Prob. 21.2PCh. 21 - Give the IUPAC name for each aldehyde.Ch. 21 - Prob. 21.4PCh. 21 - Give the IUPAC name for each ketone.Ch. 21 - Prob. 21.6PCh. 21 - Prob. 21.7PCh. 21 - The boiling point of is significantly higher than...Ch. 21 - Which carbonyl group in each pair absorbs at a...Ch. 21 - Problem 21.10 Draw the structure of all...
Ch. 21 - Prob. 21.11PCh. 21 - Prob. 21.12PCh. 21 - Prob. 21.13PCh. 21 - Prob. 21.14PCh. 21 - Problem 21.15 Draw the product of each...Ch. 21 - Prob. 21.16PCh. 21 - Problem 21.17 Draw the products of the following...Ch. 21 - Problem 21.18 Outline a synthesis of each Wittig...Ch. 21 - Problem 21.19 Draw the products (including...Ch. 21 - Problem 21.20 What starting materials are needed...Ch. 21 - Prob. 21.21PCh. 21 - Problem 21.22 The product formed when reacts with...Ch. 21 - Prob. 21.23PCh. 21 - Prob. 21.24PCh. 21 - Prob. 21.25PCh. 21 - Prob. 21.26PCh. 21 - Prob. 21.27PCh. 21 - Problem 21.28 Draw a stepwise mechanism for the...Ch. 21 - Problem 21.29 Draw the products of each...Ch. 21 - Problem 21.30 Label each compound as an acetal, a...Ch. 21 - Problem 21.31 Draw a stepwise mechanism for the...Ch. 21 - Problem 21.32 Draw the products of each...Ch. 21 - Problem 21.33 Safrole is a naturally occurring...Ch. 21 - Prob. 21.34PCh. 21 - Problem 21.35 How would you use a protecting group...Ch. 21 - Prob. 21.36PCh. 21 - Problem 21.37 Two naturally occurring compounds...Ch. 21 - Problem 21.38 Draw the products of each...Ch. 21 - Prob. 21.39PCh. 21 - Problem 21.40 (a) Give the IUPAC name for A and B....Ch. 21 - 21.41 Rank the following compounds in order of...Ch. 21 - Prob. 21.42PCh. 21 - 21.43 Give the IUPAC name for each compound.
a....Ch. 21 - 21.44 Give the structure corresponding to each...Ch. 21 - Prob. 21.45PCh. 21 - 21.46 Draw the products of each reaction.
a. e....Ch. 21 - Prob. 21.47PCh. 21 - 21.48 Draw all stereoisomers formed in each...Ch. 21 - Prob. 21.49PCh. 21 - What products are formed when each acetal is...Ch. 21 - Prob. 21.51PCh. 21 - Prob. 21.52PCh. 21 - Which compound forms the higher concentration of...Ch. 21 - Prob. 21.54PCh. 21 - Prob. 21.55PCh. 21 - Prob. 21.56PCh. 21 - Prob. 21.57PCh. 21 - Devise a synthesis of each alkene using a Wittig...Ch. 21 - Devise a synthesis of each compound from...Ch. 21 - Prob. 21.60PCh. 21 - Devise a synthesis of each compound from ethanol...Ch. 21 - Prob. 21.62PCh. 21 - Prob. 21.63PCh. 21 - 21.64 Draw a stepwise mechanism for the following...Ch. 21 - 21.65 Draw a stepwise mechanism f or the following...Ch. 21 - Prob. 21.66PCh. 21 - 21.67 Draw a stepwise mechanism for each...Ch. 21 - 21.68 Draw a stepwise mechanism for the following...Ch. 21 - Prob. 21.69PCh. 21 - Prob. 21.70PCh. 21 - Prob. 21.71PCh. 21 - Prob. 21.72PCh. 21 - 21.73 Although the carbonyl absorption of cyclic...Ch. 21 - 21.74 Use the and data to determine the...Ch. 21 - 21.75 A solution of acetone in ethanol in the...Ch. 21 - Compounds A and B have molecular formula ....Ch. 21 - 21.77 An unknown compound C of molecular formula ...Ch. 21 - 21.78 An unknown compound D exhibits a strong...Ch. 21 - Prob. 21.79PCh. 21 - -D-Glucose, a hemiacetal, can be converted to a...Ch. 21 - 21.81 Draw a stepwise mechanism for the following...Ch. 21 - Prob. 21.82PCh. 21 - 21.83 Draw a stepwise mechanism f or the...Ch. 21 - Prob. 21.84PCh. 21 - Prob. 21.85PCh. 21 - 21.86 Draw stepwise mechanism for the following...
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- 14.34 Draw all reasonable resonance structures for each species. a. b. Ö :0: C. :0: :0: d. OH e. f. :O:arrow_forward7. The standard reduction potentials for two half-reactions are shown above. Which of the statements listed below will be true for the following reaction taking place under standard conditions? a. E° b. E° c. E° = d. E° e. E° = Al (s) + Cr³+ → Al³+ + Cr (s) 0.93 V, and the reaction is not spontaneous 0.93 V, and the reaction is spontaneous 2.39 V, and the reaction is not spontaneous 2.39 V, and the reaction is not spontaneous 0.93 V, and the reaction is spontaneous Cu2+ + 2e → Cu E° = +0.34 V Zn2+ + 2e → Zn E° = -0.76 V E° = -1.18 V Mn2+ + 2e → Mn 8. Based on the above reduction potential, which of the following reactions will occur spontaneously? a. Mn²+ + Cu → Mn + Cu2+ b. Mn²+ + Zn → Mn + Zn²+ c. Zn2+ + Cu → Zn + Cu²+ d. Zn²+ + Mn → Zn + Mn2+ e. Cu²+ + Zn²+ → Cu + Znarrow_forward14.35 For which compounds can a second resonance structure be drawn? Draw an additional resonance structure and the hybrid for each resonance-stabilized compound. a. OCH3 OCH 3 b. C. d. CH3 NHCH3arrow_forward
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