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Hydrocarbons - Constitutional Isomers of C5H12 Video Lecture - Class 11

FAQs on Hydrocarbons - Constitutional Isomers of C5H12 Video Lecture - Class 11

1. What are constitutional isomers of C5H12?
Ans. Constitutional isomers of C5H12 are different compounds that have the same molecular formula (C5H12) but differ in the arrangement of atoms within the molecule. They have different structural formulas and different chemical properties.
2. How many constitutional isomers are possible for C5H12?
Ans. For C5H12, there are three constitutional isomers possible: pentane, 2-methylbutane, and 2,2-dimethylpropane. These isomers have different structural formulas but the same molecular formula.
3. What is the difference between structural isomers and stereoisomers?
Ans. Structural isomers, also known as constitutional isomers, have the same molecular formula but differ in the arrangement of atoms within the molecule. Stereoisomers, on the other hand, have the same molecular formula and the same connectivity of atoms but differ in their spatial arrangement.
4. How can constitutional isomers be identified?
Ans. Constitutional isomers can be identified by comparing their structural formulas. If two compounds have the same molecular formula but different arrangements of atoms, they are constitutional isomers. Analyzing the connectivity and positioning of atoms in the molecule helps in distinguishing between different constitutional isomers.
5. What are some examples of constitutional isomers in other hydrocarbon classes?
Ans. In addition to C5H12, there are numerous examples of constitutional isomers in other hydrocarbon classes. For example, in the C4H10 class, there are two constitutional isomers: butane and isobutane. In the C6H14 class, there are five constitutional isomers: hexane, 2-methylpentane, 3-methylpentane, 2,2-dimethylbutane, and 2,3-dimethylbutane. These isomers exhibit different structural formulas and have different physical and chemical properties.
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