Answer
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Hint: We know that isomers are different in physical and chemical properties but have the same number of atoms. This phenomenon is termed as isomerism.
Complete step by step answer:
Structural isomers are those isomers where atoms are fully arranged with the same molecular formulae in different order. Molecular formula of Cyclohexane, methylcyclopentane, 1, 3-dimethyl cyclobutane and 1, 2, 3- trimethyl cyclopropane is ${{\rm{C}}_{\rm{6}}}{{\rm{H}}_{{\rm{12}}}}$.
Cyclohexane has 6 carbon and 12 hydrogen atoms. Now we draw structure of cyclohexane is as follows:
Methylcyclopentane has 6 carbon and 12 hydrogen atoms. Now we draw structure of methylcyclopentane is as follows:
1, 3-dimethyl cyclobutane has 6 carbon and 12 hydrogen atoms. Now we draw structure of 1, 3-dimethyl cyclobutane is as follows:
1, 2, 3- trimethyl cyclopropane has 6 carbon and 12 hydrogen atoms. Now we draw structure of 1, 2, 3- trimethyl cyclopropane is as follows:
Structural isomers are also termed as constitutional isomers. Constitutional isomers have the same molecular formula but numbering and IUPAC names are different. Only count the number of each atom in both molecules to see how atoms are organized to decide whether two molecules are constitutional isomers.
Position isomers are also structural or constitutional isomers with the same functional group and same carbon skeleton but differing in position of the same functional group on or inside the carbon chain.
Cyclohexane, methylcyclopentane, 1, 3-dimethyl cyclobutane and 1, 2, 3- trimethyl cyclopropane are structural isomers because they have same molecular formula $\left( {{{\rm{C}}_{\rm{6}}}{{\rm{H}}_{{\rm{12}}}}} \right)$ but different bonding arrangement.
Hence, the correct answer is C.
Note:
Isomers are classified as structural (constitutional) and stereoisomerism. Structural isomers are further classified as chain isomers, position isomers and functional group isomers.
Complete step by step answer:
Structural isomers are those isomers where atoms are fully arranged with the same molecular formulae in different order. Molecular formula of Cyclohexane, methylcyclopentane, 1, 3-dimethyl cyclobutane and 1, 2, 3- trimethyl cyclopropane is ${{\rm{C}}_{\rm{6}}}{{\rm{H}}_{{\rm{12}}}}$.
Cyclohexane has 6 carbon and 12 hydrogen atoms. Now we draw structure of cyclohexane is as follows:
Methylcyclopentane has 6 carbon and 12 hydrogen atoms. Now we draw structure of methylcyclopentane is as follows:
1, 3-dimethyl cyclobutane has 6 carbon and 12 hydrogen atoms. Now we draw structure of 1, 3-dimethyl cyclobutane is as follows:
1, 2, 3- trimethyl cyclopropane has 6 carbon and 12 hydrogen atoms. Now we draw structure of 1, 2, 3- trimethyl cyclopropane is as follows:
Structural isomers are also termed as constitutional isomers. Constitutional isomers have the same molecular formula but numbering and IUPAC names are different. Only count the number of each atom in both molecules to see how atoms are organized to decide whether two molecules are constitutional isomers.
Position isomers are also structural or constitutional isomers with the same functional group and same carbon skeleton but differing in position of the same functional group on or inside the carbon chain.
Cyclohexane, methylcyclopentane, 1, 3-dimethyl cyclobutane and 1, 2, 3- trimethyl cyclopropane are structural isomers because they have same molecular formula $\left( {{{\rm{C}}_{\rm{6}}}{{\rm{H}}_{{\rm{12}}}}} \right)$ but different bonding arrangement.
Hence, the correct answer is C.
Note:
Isomers are classified as structural (constitutional) and stereoisomerism. Structural isomers are further classified as chain isomers, position isomers and functional group isomers.
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