Organic Chemistry - Standalone book
Organic Chemistry - Standalone book
10th Edition
ISBN: 9780073511214
Author: Francis A Carey Dr., Robert M. Giuliano
Publisher: McGraw-Hill Education
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Chapter 15.13, Problem 19P

The product of the following reaction was isolated in 99 % yield. What is it?

Chapter 15.13, Problem 19P, The product of the following reaction was isolated in 99 yield. What is it?

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4d please give the resulting product and explain
Nucleophilic substitution happens on compounds having nucleophilic groups as leaving groups. The rule is, the weaker the basicity of a group of the substrate, the better is its leaving ability. In these substitution reactions, the basicity of leaving group must be less than the incoming nucleophilic group. Nucleophilic substitution reaction at sp3-hybridized carbon is either bimolecular (SN2) or unimolecular. Bimolecular reaction takes place in single step, involving transition state intermediate. In SN2 reaction, inversion in configuration occurs. In case of optically active alkyl halides, the inversion in configuration is called Walden inversion. SN2 reaction is preferred if the compound has less steric hindrance. On the other hand, unimolecular (SN1) reaction involves two steps and a carbonium ion intermediate. Optically active substrates give racemic mixture in these type of reactions. Which of the following will produce enantiomeric pair on treatment with HOH? " I ÇH, C,Hs-C-Br…
The oxygen in water is primarily (99.8%) 16O, but water enriched with theheavy isotope 18O is also available. When a ketone or aldehyde is dissolved inH2O, the isotopic label becomes incorporated into the carbonyl group: R2CPO H2O n R2CPO  H2O. Explain.

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