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The 43 pages that link to Cis–trans isomerism, each with the reason it gives.

• Fatty acidRelated: Double-bond geometry bends some chains and changes their packing.

• AlkeneRelated: Restricted rotation around an alkene double bond can produce distinct cis and trans forms.

• Pi bondRelated: Restricted rotation around a carbon–carbon pi bond can preserve distinct geometric isomers.

• Saturated fatRelated: Unlike unsaturated chains, saturated chains have no double bond that can create cis or trans forms.

• Dietary fatRelated: Double-bond geometry distinguishes many natural unsaturated fats from industrial trans fats.

• Oleic acidRelated: Oleic acid’s cis geometry bends its chain and distinguishes it from elaidic acid.

• DiastereomerRelated: Cis and trans forms can be diastereomers despite having no stereogenic centers.

• Dicarboxylic acidRelated: Cyclic dicarboxylic acids can have distinct cis and trans arrangements of their carboxyl groups.

• Trans fatRelated: The trans configuration distinguishes these fatty acids from their more common cis counterparts.

• EpoxideRelated: Substituents on an epoxide ring can have distinct cis and trans arrangements.

• Stereospecific reactionRelated: Reactant geometry such as cis or trans can dictate product geometry.

• Styrene-butadiene rubberRelated: Butadiene's incorporation geometry affects chain flexibility and the properties of SBR.

• Monounsaturated fatRelated: The geometry of a fatty acid’s single double bond affects its shape and physical properties.

• PolyisopreneRelated: The geometry of each double bond distinguishes flexible natural rubber from rigid gutta-percha.

• Polyunsaturated fatty acidRelated: The geometry of each double bond bends or straightens the chain.

• ButadieneRelated: The geometry of residual double bonds affects the properties of polybutadiene.

• Fumaric acidRelated: Fumaric acid is the trans isomer of butenedioic acid.

• Alfred WernerRelated: Different arrangements of ligands in cobalt complexes matched the geometries Werner proposed.

• Double bondRelated: The rotational restriction of double bonds can preserve distinct substituent arrangements.

• Fused ringRelated: Groups at a ring junction can lie on the same or opposite faces.

• ProlineRelated: Proline-containing peptide bonds switch between cis and trans forms more often than most peptide bonds.

• Aliphatic compoundRelated: Double bonds and rings can restrict rotation in aliphatic structures.

• AzobenzeneRelated: The N=N bond gives azobenzene its two principal geometric isomers.

• Palmitoleic acidRelated: The naturally common form of palmitoleic acid has cis geometry at its double bond.

• Coordination sphereRelated: Different ligand arrangements within a sphere can produce distinct cis and trans compounds.