Linked from

The 53 pages that link to Alcohol, each with the reason it gives.

• EsterRelated: Alcohols supply the oxygen-linked carbon group in common esterification reactions.

• GABARelated: Alcohol can alter GABA_A receptor signaling, contributing to sedation and impaired coordination.

• Dehydration reactionRelated: Alcohols are common substrates for acid-catalyzed dehydration to alkenes.

• EnolRelated: Enols contain a hydroxyl group, but its attachment to an alkene carbon changes its behavior.

• Grignard reagentRelated: Workup of Grignard addition to carbonyl compounds commonly produces alcohols.

• Hydration reactionRelated: Many organic hydration reactions convert an alkene into an alcohol.

• Condensation reactionRelated: Its hydroxyl group can combine with an acid-derived group during ester-forming condensation.

• Fischer esterificationRelated: Its oxygen becomes the ester’s single-bonded oxygen.

• Sodium borohydrideRelated: Aldehyde and ketone reductions commonly produce alcohols.

• Williamson ether synthesisRelated: Deprotonating an alcohol commonly produces the alkoxide coupling partner.

• Phosphorus pentachlorideRelated: PCl₅ can replace an alcohol’s hydroxyl group with chlorine, though other reagents are often preferred.

• LinaloolRelated: Linalool’s hydroxyl group makes it a terpene alcohol.

• Herbert C. BrownRelated: Hydroboration followed by oxidation offers a reliable route from alkenes to alcohols.

• GeraniolRelated: Geraniol’s hydroxyl group defines its alcohol functionality.

• Tincture of iodineRelated: Alcohol serves as the tincture’s solvent and adds its own antimicrobial and irritating effects.