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

34. Nucleic Acids

Intro to Nucleic Acids

Organic Chemistry

34. Nucleic Acids

Intro to Nucleic Acids

Previous problemNext problem

Struggling with Organic Chemistry?

Join thousands of students who trust us to help them ace their exams!Watch the first video

Multiple Choice

Which of the following tools of DNA technology is incorrectly paired with its use?

DNA ligase - Joining DNA fragments together

Gel electrophoresis - Separating DNA fragments by size

Restriction enzymes - Cutting DNA at specific sequences

PCR - Sequencing DNA

Previous problemNext problem

Verified step by step guidance

Understand the role of each tool in DNA technology: DNA ligase, gel electrophoresis, restriction enzymes, and PCR.

DNA ligase is an enzyme that facilitates the joining of DNA strands together by catalyzing the formation of a phosphodiester bond. It is correctly paired with joining DNA fragments.

Gel electrophoresis is a technique used to separate DNA fragments based on their size. DNA fragments are loaded into a gel and an electric current is applied, causing the fragments to move through the gel. Smaller fragments move faster than larger ones, allowing for separation by size. This is correctly paired.

Restriction enzymes are proteins that cut DNA at specific sequences, known as restriction sites. They are used to cut DNA into smaller fragments for analysis or recombination. This is correctly paired.

PCR (Polymerase Chain Reaction) is a technique used to amplify a specific segment of DNA, making millions of copies of a particular DNA sequence. It is not used for sequencing DNA, which involves determining the exact order of nucleotides in a DNA molecule. Therefore, PCR is incorrectly paired with sequencing DNA.