Organic Chemistry As a Second Language: First Semester Topics
Organic Chemistry As a Second Language: First Semester Topics
4th Edition
ISBN: 9781119110668
Author: David R. Klein
Publisher: WILEY
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Chapter 12.3, Problem 12.12P
Interpretation Introduction

Interpretation:

The reagents necessary to achieve the given transformation has to be identified.

Concept Introduction:

Alkynes are the compounds that contain a triple bond between two carbon atoms.  The carbon atom present in the triple bond is sp hybridised.  Due to this, the geometry of alkyne will be linear.  Terminal alkyne are the one which has a proton attached to the triple bond and internal alkyne are the one in which there are no protons attached to the triple bond.

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.3, Problem 12.12P , additional homework tip  1

The terminal alkynes can be deprotonated upon treatment with a strong base such as sodium amide to give an alkynide ion.  Alkynide ions are very strong nucleophiles and can take part in SN2 reaction, when treated with electrophile.  The electrophile may be only primary halide because elimination reaction will be favored in case of secondary and tertiary halide.

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.3, Problem 12.12P , additional homework tip  2

If the starting alkyne is acetylene, then the installation of the alkyl groups has to be done one at one time.  This means that one group is installed on one side and then the second substitution takes place in next step.

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.3, Problem 12.12P , additional homework tip  3

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10:04 AM Tue Mar 25 Sunday 9:30 AM 95% Edit Draw the corresponding structures in each of the boxes below: Ester Name Methyl butyrate (Example) Alcohol Structure H3C-OH Acid Structure Ester Structure Isoamyl acetate Ethyl butyrate Propyl acetate Methyl salicylate Octyl acetate Isobutyl propionate Benzyl butyrate Benzyl acetate Ethyl acetate H₂C OH HC
2) For each of the following reactions: (i) (ii) Fill in the missing reactant, reagent, or product (s), indicating stereochemistry where appropriate using dashed and wedged bonds. If the reaction forms a racemic mixture, draw both structures in the box and write the word "racemic". (a) (b) 1) R₂BH 2) H₂O2, NaOH (aq) HBr Br racemic Br + Br Br racemic
For each of the following reactions:  Fill in the missing reactant, reagent, or product (s), indicating stereochemistry where appropriate using dashed and wedged bonds. If the reaction forms a racemic mixture, draw both structures in the box and write the word “racemic”.
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