The Newman projection has to be drawn and the reason has to be explained for the formation of more trans product. Concept introduction: Conformations: Rotation about C-C single bonds allows a compound to adopt a variety of possible three-dimensional shapes. Newman projections: The new conformations of compounds can be drawn and analyzed by Newman projections. A Newman projection visualizes different conformations of Carbon-carbon chemical bond from front to back with the front carbon represented as a black dot and the back represented as a circle. The angle between two hydrogens of a Newman projection is called as dihedral angle or torsional angle. This dihedral angle changes as the C-C bond rotates. Two conformations with special attentions are staggered and eclipsed conformation. Staggered conformation is the lowest in energy and the eclipsed conformation is the highest in energy. For example, Anti-conformation: The conformation with a dihedral angle of is called anti-conformation. The two methyl groups achieve maximum separation from each other. In other, methyl groups are closer to each other; their electron clouds are repelling each other, causing an increase in energy. This unfavorable interaction is called gauche interaction. E2 elimination: Alkyl halide forms an alkene from the abstraction of the proton from the β-carbon atom followed by elimination of the halogen in a single step.

Question

Part 1. Draw monomer units of the following products and draw their reaction mechanism 1) Bakelite like polymer Using: Resorcinol + NaOH + Formalin 2) Polyester fiber Using a) pthalic anhydride + anhydrous sodium acetate + ethylene glycol B)pthalic anhydride + anhydrous sodium acetate + glycerol 3) Temporary cross-linked polymer Using: 4% polyvinyl alcohol+ methyl red + 4% sodium borate

Answer 1

Question

Chapter 11.SE, Problem 51AP

Interpretation Introduction

Interpretation:

The Newman projection has to be drawn and the reason has to be explained for the formation of more trans product.

Concept introduction:

Conformations: Rotation about C-C single bonds allows a compound to adopt a variety of possible three-dimensional shapes.

Newman projections: The new conformations of compounds can be drawn and analyzed by Newman projections. A Newman projection visualizes different conformations of Carbon-carbon chemical bond from front to back with the front carbon represented as a black dot and the back represented as a circle.

The angle between two hydrogens of a Newman projection is called as dihedral angle or torsional angle. This dihedral angle changes as the C-C bond rotates. Two conformations with special attentions are staggered and eclipsed conformation. Staggered conformation is the lowest in energy and the eclipsed conformation is the highest in energy.

For example,

Anti-conformation: The conformation with a dihedral angle of is called anti-conformation.

The two methyl groups achieve maximum separation from each other. In other, methyl groups are closer to each other; their electron clouds are repelling each other, causing an increase in energy. This unfavorable interaction is called gauche interaction.

E2 elimination:

Alkyl halide forms an alkene from the abstraction of the proton from the β-carbon atom followed by elimination of the halogen in a single step.

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