Table of contents

1. A Review of General Chemistry5h 5m
2. Molecular Representations1h 14m
3. Acids and Bases2h 46m
4. Alkanes and Cycloalkanes4h 17m
5. Chirality3h 39m
6. Thermodynamics and Kinetics1h 22m
7. Substitution Reactions1h 48m
8. Elimination Reactions2h 30m
9. Alkenes and Alkynes2h 9m
10. Addition Reactions3h 19m
11. Radical Reactions1h 58m
12. Alcohols, Ethers, Epoxides and Thiols2h 42m
13. Alcohols and Carbonyl Compounds2h 17m
14. Synthetic Techniques1h 26m
15. Analytical Techniques:IR, NMR, Mass Spect7h 3m
16. Conjugated Systems6h 13m
17. Ultraviolet Spectroscopy51m
18. Aromaticity2h 34m
19. Reactions of Aromatics: EAS and Beyond5h 1m
20. Phenols55m
21. Aldehydes and Ketones: Nucleophilic Addition4h 56m
22. Carboxylic Acid Derivatives: NAS2h 51m
23. The Chemistry of Thioesters, Phophate Ester and Phosphate Anhydrides1h 10m
24. Enolate Chemistry: Reactions at the Alpha-Carbon1h 53m
25. Condensation Chemistry2h 9m
26. Amines1h 43m
27. Heterocycles2h 0m
28. Carbohydrates5h 53m
29. Amino Acids4h 20m
30. Peptides and Proteins2h 42m
31. Catalysis in Organic Reactions1h 30m
32. Lipids 2h 50m
33. The Organic Chemistry of Metabolic Pathways2h 52m
34. Nucleic Acids1h 32m
35. Transition Metals6h 14m
36. Synthetic Polymers1h 49m

4. Alkanes and Cycloalkanes

Cis vs Trans

Organic Chemistry

4. Alkanes and Cycloalkanes

Cis vs Trans

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Multiple Choice

Determine the IUPAC name of the following molecule

5-bromo-5-fluoro-3-heptene

3-bromo-3-ethyl-3-fluoro-5-hexene

4-bromo-2-ethyl-4-fluoro-1-hexene

5-bromo-5-fluoro-3-methyleneheptene

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Verified step by step guidance

Identify the longest carbon chain in the molecule that contains the highest priority functional group, which in this case is the alkene group. This will determine the base name of the compound.

Number the carbon atoms in the longest chain starting from the end nearest to the highest priority functional group, which is the double bond in this case. This ensures the lowest possible numbers for the substituents and the double bond.

Identify and name all substituents attached to the main carbon chain. In this molecule, the substituents include bromo, fluoro, and ethyl groups.

Assign a number to each substituent based on its position on the main carbon chain. Ensure that the substituents are listed in alphabetical order in the final name, regardless of their position numbers.

Combine the names and numbers of the substituents with the base name of the compound, ensuring that the position of the double bond is indicated by the lowest possible number. The final IUPAC name should reflect the correct structure and substituent positions.