Organic Chemistry
Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
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Chapter 29.SE, Problem 26MP
Interpretation Introduction

Interpretation:

A mechanism for the conversion of fumaroylacetoacetate to fumarate plus acetoacetate.

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f) The unusual molecule [2.2.2] propellane is pictured. 1) Given the bond length and bond angles in the image, what hybridization scheme best describes the carbons marked by the askerisks? 2) What types of orbitals are used in the bond between the two carbons marked by the askerisks? 3) How does this bond compare to an ordinary carbon-carbon bond (which is usually 1.54 Å long)? CH2 1.60Å H2C た C CH2 H2C H₂C * 120° C H2
Denote the dipole for the indicated bonds in the following molecules. H3C CH3 B F-CCl3 Br-Cl | H3C Si(CH3)3 OH НО. HO H O HO OH vitamin C CH3
Q2: Draw all applicable resonance forms for the acetate ion CH3COO. Clearly show all lone pairs, charges, and arrow formalism.

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