Organic Chemistry-Package(Custom)
4th Edition
ISBN: 9781259141089
Author: SMITH
Publisher: MCG
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Chapter 31, Problem 31.12P
What
a. 
b. 
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Why doesn't this carry on to form a ring by deprotonating the alpha carbon and the negatively-charged carbon attacking the C=O?
6. A solution (0.0004 M) of Fe(S2CNEt2)3 (see the structural drawing below) in chloroform
has absorption bands at:
350 nm (absorbance A = 2.34);
514 nm(absorbance A = 0.0532);
Calculate the molar absorptivity values for these bands. Comment
on their possible nature (charge transfer transitions or d-d
S
N-
transitions?).
(4 points)
What is the mechanism for this?
Chapter 31 Solutions
Organic Chemistry-Package(Custom)
Ch. 31 - Prob. 31.1PCh. 31 - Prob. 31.2PCh. 31 - Prob. 31.3PCh. 31 - Draw the mechanism for the radical polymerization...Ch. 31 - Prob. 31.5PCh. 31 - Prob. 31.6PCh. 31 - Prob. 31.7PCh. 31 - Prob. 31.8PCh. 31 - Prob. 31.9PCh. 31 - Prob. 31.10P
Ch. 31 - Prob. 31.11PCh. 31 - Problem 30.12
What polymer is formed by anionic...Ch. 31 - Prob. 31.13PCh. 31 - Prob. 31.14PCh. 31 - Problem 30.15
What polyamide is formed from each...Ch. 31 - Prob. 31.16PCh. 31 - Prob. 31.17PCh. 31 - Prob. 31.18PCh. 31 - Prob. 31.19PCh. 31 - Prob. 31.20PCh. 31 - Prob. 31.21PCh. 31 - Prob. 31.22PCh. 31 - Prob. 31.23PCh. 31 - Prob. 31.24PCh. 31 - Prob. 31.25PCh. 31 - Prob. 31.26PCh. 31 - 30.26 Draw the structure of the polymer formed by...Ch. 31 - Prob. 31.28PCh. 31 - Prob. 31.29PCh. 31 - Prob. 31.30PCh. 31 - Prob. 31.31PCh. 31 - Prob. 31.32PCh. 31 - Prob. 31.33PCh. 31 - Prob. 31.34PCh. 31 - Prob. 31.35PCh. 31 - Prob. 31.36PCh. 31 - Prob. 31.37PCh. 31 - Prob. 31.38PCh. 31 - Prob. 31.39PCh. 31 - 30.39 Draw a stepwise mechanism for the...Ch. 31 - 30.40 Cationic polymerization of 3-phenylpropene ...Ch. 31 - Prob. 31.42PCh. 31 - Prob. 31.43PCh. 31 - 30.43 Although styrene undergoes both cationic and...Ch. 31 - 30.44 Rank the following compounds in order of...Ch. 31 - Prob. 31.46PCh. 31 - Prob. 31.47PCh. 31 - 30.47 Draw a stepwise mechanism for the following...Ch. 31 - 30.48 Draw a stepwise mechanism for the reaction...Ch. 31 - Prob. 31.50PCh. 31 - Prob. 31.51PCh. 31 - Prob. 31.52PCh. 31 - 30.52 (a) Explain why poly (vinyl alcohol) cannot...Ch. 31 - Prob. 31.54PCh. 31 - 30.53 Devise a synthesis of terephthalic acid and...Ch. 31 - Prob. 31.56PCh. 31 - Prob. 31.57PCh. 31 - 30.56 Compound A is a novel poly (ester amide)...Ch. 31 - Researchers at Rutgers University have developed...Ch. 31 - 30.58 Melmac, a thermosetting polymer formed from...Ch. 31 - 30.59 Although chain branching in radical...Ch. 31 - Prob. 31.62P
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- For questions 1-4, consider the following complexes: [Co(CN)6], [COC14]², [Cr(H2O)6]²+ 4. Room temperature (20°C) measurement of molar magnetic susceptibility (Xm) for Fe(NH4)2(SO4)2×6H2O is 1.1888 x 102 cgs (Gaussian units). Calculate effective magnetic moment and provide a number of unpaired electrons for the iron ion. Use this number to rationalize the coordination geometry around iron center. (4 points)arrow_forward7. Describe the expected 31P and 19F (where applicable) NMR spectral patterns for the following compounds (indicate number of signals and their splitting patterns). a) tetraphenyldiphosphine Ph Ph P-P Ph Ph Ph Ph ' b) tetraphenyldiphosphine monoxide P-P-Ph Ph (2 points) (2 points c) tetrafluorophosphonium hexafluorophosphate [PF4]*[PF6]¯ (4 points)arrow_forward3. For questions 1-4, consider the following complexes: [Co(CN)6]4, [COC14]², [Cr(H2O)6]²+ Which (if any) of these complexes would be expected to display Jahn-Teller distortion? (2 points)arrow_forward
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