CHS Module 8 Video 2 Thiols, Aldehydes, Ketones
Introduction to Organic Chemistry: Sulfur Compounds
Focus on thiols, aldehydes, and ketones.
Thiols
Definition and Structure
Also known as mercaptans.
Characterized by the presence of a sulfur-hydrogen group (–SH).
Systematic naming: Add "thiol" to the parent hydrocarbon name.
Characteristics
Notable for their strong, unpleasant odor (e.g., skunk, garlic, onions).
Use in natural gas: Thiols are added for odor detection to prevent accidents.
Biological Importance
Occur in the amino acid cysteine.
Cysteine is integral to protein structure due to the formation of disulfide bonds.
Reactions
React with mild oxidizing agents to form disulfides (–S–S–).
Disulfide bonds: Two thiols combine, losing hydrogen atoms and linking sulfurs.
Revoked by reducing agents, which add hydrogens back.
Examples in Biology
Proteins, including hair, are rich in disulfide bonds contributing to structural integrity.