Ch. 14 - Synthetic TechniquesWorksheetSee all chapters
All Chapters
Ch. 1 - A Review of General Chemistry
Ch. 2 - Molecular Representations
Ch. 3 - Acids and Bases
Ch. 4 - Alkanes and Cycloalkanes
Ch. 5 - Chirality
Ch. 6 - Thermodynamics and Kinetics
Ch. 7 - Substitution Reactions
Ch. 8 - Elimination Reactions
Ch. 9 - Alkenes and Alkynes
Ch. 10 - Addition Reactions
Ch. 11 - Radical Reactions
Ch. 12 - Alcohols, Ethers, Epoxides and Thiols
Ch. 13 - Alcohols and Carbonyl Compounds
Ch. 14 - Synthetic Techniques
Ch. 15 - Analytical Techniques: IR, NMR, Mass Spect
Ch. 16 - Conjugated Systems
Ch. 17 - Aromaticity
Ch. 18 - Reactions of Aromatics: EAS and Beyond
Ch. 19 - Aldehydes and Ketones: Nucleophilic Addition
Ch. 20 - Carboxylic Acid Derivatives: NAS
Ch. 21 - Enolate Chemistry: Reactions at the Alpha-Carbon
Ch. 22 - Condensation Chemistry
Ch. 23 - Amines
Ch. 24 - Carbohydrates
Ch. 25 - Phenols
Ch. 26 - Amino Acids, Peptides, and Proteins

Solution: Provide an efficient multistep synthesis for the following conversion of the given starting compound into the target compound. For this problem, do not give a mechanism with curved arrows. For the synthesis, more than one functional group transformation is required. For each functional group transformation, give all necessary reagents and catalysts and give a structural formula of the organic product. Also give hv and/or heat when necessary. Show stereochemistry appropriately when necessary. 

Problem

Provide an efficient multistep synthesis for the following conversion of the given starting compound into the target compound. For this problem, do not give a mechanism with curved arrows. For the synthesis, more than one functional group transformation is required. For each functional group transformation, give all necessary reagents and catalysts and give a structural formula of the organic product. Also give hv and/or heat when necessary. Show stereochemistry appropriately when necessary.