Q2. Show how each of the following compound can be produced from an alkene or alkyne(dihydroxylation, oxidative cleavage):(a)1. conc KMnO4,KOH, A2. HO(b)1. conc KMnO4,KOH, A(c)??1.03,-78 °C?2. HO2. Zn, HOAc(d)1.03, -78 °C2. H₂O2?(e)1. OsO4H2O22. HIO4(1)?HOconc KMnOKOH, A?

Dear student,Below is the answer and explanation to your assignment:Part 1: Answer(a) 1. 1,2-diol…

Answered: Q2. Show how each of the following…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter24: Amines And Heterocycles

Section24.9: Heterocyclic Amines

Problem 24P

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Could someone help me with ranking these with how reactive they would be with an SN2 reaction? Thanks :)
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In some nucleophilic substitutions under SN1 conditions, complete racemization does not occur and a small excess of one enantiomer ispresent. For example, treatment of optically pure 1-bromo-1phenylpropane with water forms 1-phenylpropan-1-ol. (a) Calculate how much of each enantiomer is present using the given optical rotation data. (b) Which product predominates—the product of inversion or the product of retention of configuration? (c) Suggest an explanation for this phenomenon.

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