For the given structures the multiplicity of each signal to be identified. Concept Introduction : Multiplicity: The number of peaks on the each signal in NMR spectrum is defined as multiplicity; the multiplicity of each signal indicates the neighboring protons. It is generated by coupling of the subjected protons with the neighboring protons (both subjected and neighbor protons are to be chemically not equivalent) separated by either two or three sigma bonds. Rule : Multiplicity of each signal is calculated using (n+1) rule only when the neighboring protons are chemically equivalent to each other. (n+1) where n indicates number of neighboring protons

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Consider the following nucleophilic substitution reaction. The compound listed above the arrow is the solvent for the reaction. If nothing is listed over the arrow, then the nucleophile is also the solvent for the reaction. Part 1 of 2 Br CH,CN + I¯ What is the correct mechanism for the reaction? Select the single best answer. @SN2 ○ SN 1 Part: 1/2 Part 2 of 2 Draw the products for the reaction. Include both the major organic product and the inorganic product. If more than one stereoisomer is possible, draw only one stereoisomer. Include stereochemistry where relevant. Click and drag to start drawing a structure. X હૈ

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Chapter 15.7, Problem 5LTS

Interpretation Introduction

Interpretation: For the given structures the multiplicity of each signal to be identified.

Concept Introduction:

Multiplicity: The number of peaks on the each signal in NMR spectrum is defined as multiplicity; the multiplicity of each signal indicates the neighboring protons. It is generated by coupling of the subjected protons with the neighboring protons (both subjected and neighbor protons are to be chemically not equivalent) separated by either two or three sigma bonds.

Rule: Multiplicity of each signal is calculated using (n+1) rule only when the neighboring protons are chemically equivalent to each other.

(n+1)where n indicates number of neighboring protons

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