In the molecule C6H12, we can observe structural isomerism, specifically chain isomerism and positional isomerism. Here are some examples of isomers for C6H12:1. Hex-1-ene Chain isomer H2C=CH-CH2-CH2-CH2-CH32. Hex-2-ene Chain isomer CH3-CH=CH-CH2-CH2-CH33. 3-Methylpent-1-ene Positional isomer CH3-CH=CH-CH CH3 -CH2-CH34. 2-Methylpent-2-ene Positional isomer CH3-C CH3 =CH-CH2-CH2-CH35. Cyclohexane Ring isomer -CH2-CH2-CH2-CH2-CH2-CH2-6. Methylcyclopentane Ring isomer CH3 | -CH2-CH2-CH2-CH2-CH2-In these examples, chain isomerism occurs when the carbon atoms are connected in different ways, forming different carbon chains. For example, hex-1-ene and hex-2-ene have different carbon chain structures.Positional isomerism occurs when the position of the functional group in this case, the double bond changes within the same carbon chain. For example, 3-methylpent-1-ene and 2-methylpent-2-ene have the same carbon chain but different positions for the double bond.Ring isomerism occurs when the carbon atoms are connected in a ring structure, such as in cyclohexane and methylcyclopentane.