Organic Chemistry: Principles And Mechanisms
Organic Chemistry: Principles And Mechanisms
2nd Edition
ISBN: 9780393663549
Author: KARTY, Joel
Publisher: W. W. Norton and Company
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Chapter 12, Problem 12.18P
Interpretation Introduction

Interpretation:

The reactant which can be epoxidized using MCPBA to get the given compound is to be determined.

Concept introduction:

MCPBA contains a peroxycarboxylic acid (-COOOH) group, which acts as an electrophile. The oxygen atom from this group simultaneously forms bonds to both carbon atoms of the alkene double bond to form an epoxide (oxirane) ring. The π electron pair from the double bond forms one bond, while one of the lone pairs of the oxygen atom forms the other bond. The result is a replacement of the π bond with two σ bonds.

The cis-trans stereochemistry about the carbon-carbon double bond is retained in the reaction.

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5) Consider the reaction: Cl2 (g) + F2 (g) ⟷ 2 ClF (g) KP=? The partial pressure of 203 kPa for Cl2 and a partial pressure of 405 kPa for F2. Upon reaching equilibrium, thepartial pressure of ClF is 180 kPa. Calculate the equilibrium concentrations and then find the value for KP.
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(9 Pts) In one of the two Rare Earth element rows of the periodic table, identify an exception tothe general ionization energy (IE) trend. For the two elements involved, answer the followingquestions. Be sure to cite sources for all physical data that you use.a. (2 pts) Identify the two elements and write their electronic configurations.b. (2 pts) Based on their configurations, propose a reason for the IE trend exception.c. (5 pts) Calculate effective nuclear charges for the last electron in each element and theAllred-Rochow electronegativity values for the two elements. Can any of these valuesexplain the IE trend exception? Explain how (not) – include a description of how IErelates to electronegativity.

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Organic Chemistry: Principles And Mechanisms

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