(a) Interpretation: The number of hydrogen atoms present around each highlighted carbon atom and molecular formula of the given molecule are to be stated. Concept introduction: A skeletal structure possesses carbon atom at the intersection of any two lines and at the end of any line. Each carbon atom must have enough hydrogens to make carbon atom tetravalent.

Question

Plan the synthesis of the following compound using the starting material provided and any other reagents needed as long as carbon based reagents have 3 carbons or less. Either the retrosynthesis or the forward synthesis (mechanisms are not required but will be graded if provided) will be accepted if all necessary reagents and intermediates are shown (solvents and temperature requirements are not needed unless specifically involved in the reaction, i.e. DMSO in the Swem oxidation or heat in the KMnO4 oxidation). There may be more than one correct answer, and chemically correct steps will be accepted. Extra points will be given if correct names are provided. The points earned here will be applied to your lowest exam score! H H

Answer 1

Question

Chapter 1.8, Problem 23P

Interpretation Introduction

(a)

Interpretation: The number of hydrogen atoms present around each highlighted carbon atom and molecular formula of the given molecule are to be stated.

Concept introduction: A skeletal structure possesses carbon atom at the intersection of any two lines and at the end of any line. Each carbon atom must have enough hydrogens to make carbon atom tetravalent.

Interpretation Introduction

(b)

Interpretation: The number of hydrogen atoms present around each highlighted carbon atom and molecular formula of the given molecule are to be stated.

Concept introduction: A skeletal structure possesses carbon atom at the intersection of any two lines and at the end of any line. Each carbon atom must have enough hydrogens to make carbon atom tetravalent.

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