Ch. 4 - Alkanes and CycloalkanesWorksheetSee 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: Write bond-line formulas for each of the following naturally occurring compounds, clearly showing their stereochemistry. The worm in apples is the larval stage of the codling moth. The sex attractant of the male  moth is the 2Z,6E stereoisomer of the compound shown.

Solution: Write bond-line formulas for each of the following naturally occurring compounds, clearly showing their stereochemistry. The worm in apples is the larval stage of the codling moth. The sex attractant

Problem

Write bond-line formulas for each of the following naturally occurring compounds, clearly showing their stereochemistry.

The worm in apples is the larval stage of the codling moth. The sex attractant of the male  moth is the 2Z,6E stereoisomer of the compound shown.