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The 98 pages that link to Ammonia, each with the reason it gives.

• WaterCompared with: Like water, ammonia is polar and hydrogen-bonding, but its molecular structure and bulk properties differ.

• Tetrahedral molecular geometryCompared with: Its electron domains are tetrahedral, but its atoms form a trigonal-pyramidal molecular shape.

• Hydrogen chlorideCompared with: Ammonia reacts with hydrogen chloride to form solid ammonium chloride.

• Sodium hydroxideCompared with: Unlike sodium hydroxide, ammonia is a weak molecular base rather than a fully dissociated ionic hydroxide.

• Hydrogen storageCompared with: Ammonia can transport hydrogen chemically, but using it requires synthesis or decomposition.

• HydroxideCompared with: Ammonia accepts protons without containing hydroxide as part of its formula.

• Potassium hydroxideCompared with: Unlike KOH, ammonia is a weak molecular base rather than a fully dissociating ionic hydroxide.

• Conjugate acidCompared with: Ammonia accepts a proton to form ammonium, its conjugate acid.

• Uric acidCompared with: Ammonia is more soluble and toxic than uric acid, but requires abundant water for safe excretion.

• AmmoniumCompared with: Unlike ammonium, ammonia is neutral and can accept a proton.

• Trigonal planar molecular geometryCompared with: Its four electron domains produce a pyramidal molecular shape, not a planar one.

• EthanolamineCompared with: Unlike ammonia, ethanolamine also contains a hydroxyl group and a carbon chain.

• HydrazineCompared with: Ammonia is a simpler nitrogen hydride and a feedstock for hydrazine production.

• MethylamineCompared with: Replacing one hydrogen in ammonia with methyl gives methylamine.

• Barium hydroxideCompared with: Unlike ammonia, barium hydroxide is an ionic strong base that supplies hydroxide directly.

• DimethylamineCompared with: Replacing two ammonia hydrogens with methyl groups yields dimethylamine.

• EthylamineCompared with: Ethylamine can be viewed as ammonia with one hydrogen replaced by an ethyl group.

• Hydrogen tellurideCompared with: Its strong hydrogen bonding and comparatively high boiling point contrast with H₂Te's weak intermolecular attractions.

• TrimethylamineCompared with: Replacing ammonia's three hydrogens with methyl groups produces trimethylamine.

• Calcium cyanamideCompared with: Ammonia is the dominant industrial starting point for modern nitrogen fertilizers.

• DichlorodifluoromethaneCompared with: Ammonia was an established refrigerant with toxicity risks that helped motivate adoption of less acutely hazardous CFCs.

• HydroxylamineCompared with: Replacing one ammonia hydrogen with hydroxyl gives hydroxylamine and substantially changes its reactivity.

• GuanidineCompared with: Unlike ammonia, guanidine’s conjugate acid distributes charge over several nitrogen atoms.

• LyeCompared with: It is an alkaline cleaner, but unlike lye it is not a hydroxide salt.

• EthylenediamineCompared with: Ethylenediamine has two nitrogen donor sites, unlike ammonia’s single donor atom.

• Hydrazoic acidCompared with: Ammonia is a basic nitrogen hydride, unlike acidic HN₃.

• Properties of waterCompared with: Like water, ammonia forms hydrogen bonds, but its different structure produces different bulk properties.