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The 18 pages that link to Dehydration reaction, each with the reason it gives.

• Hydroxyl groupRelated: Alcohol dehydration can eliminate the hydroxyl group and form an alkene.

• AlcoholRelated: Acid-catalyzed alcohol dehydration commonly forms an alkene.

• HydrateRelated: Heating often converts a hydrate into a less hydrated form or an anhydrous solid.

• GlycerolRelated: Removing water from glycerol can produce acrolein, a useful diagnostic reaction.

• CalcinationRelated: Heating hydrated solids can drive off water as part of calcination.

• DecarboxylationCompared with: It is another elimination reaction, but removes water instead of a carboxyl group.

• Crystal waterRelated: Heating or drying can remove crystal water and transform the hydrated solid.

• Elimination reactionBroader topic: Alcohol dehydration is a specific elimination that produces an alkene.

• ImineRelated: Loss of water from a carbinolamine creates the carbon–nitrogen double bond.

• Hydration reactionCompared with: Dehydration often reverses a hydration reaction, such as alcohol conversion to an alkene.

• Condensation reactionRelated: It is the water-releasing form commonly used to describe condensation in biochemical reactions.

• Phosphorus oxyacidsRelated: Dehydration links phosphoric acid units and generates condensed oxyacids.

• CyclohexanolRelated: Acid-catalyzed dehydration of cyclohexanol can produce cyclohexene.

• 1-PentanolRelated: Acid-catalyzed dehydration of 1-pentanol can form pentenes.

• Allyl alcoholRelated: Removing water from glycerol historically converted it into allyl alcohol.

• 1-HexanolRelated: Acid-catalyzed dehydration can convert 1-hexanol into hexenes.

• Dinitrogen pentoxideNarrower topic: Removing water from nitric acid is a standard route to N₂O₅.

• tert-Butyl alcoholRelated: Acid-catalyzed dehydration of tert-butanol produces 2-methylpropene.