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Methane & ethane hybridization structure (Part - 15) - chemical bonding and molecular structure Video Lecture - Class 11

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FAQs on Methane & ethane hybridization structure (Part - 15) - chemical bonding and molecular structure Video Lecture - Class 11

1. What is the hybridization structure of methane and ethane?
Ans. The hybridization structure of methane is sp3 while the hybridization structure of ethane is also sp3. In both molecules, the carbon atom forms four sigma bonds with hydrogen atoms, resulting in a tetrahedral arrangement of electron pairs.
2. What is the significance of hybridization in methane and ethane?
Ans. Hybridization in methane and ethane allows for the formation of sigma bonds between carbon and hydrogen atoms. This enables the molecules to have stable structures and exhibit unique chemical properties. Hybridization also affects the shape and geometry of the molecules, influencing their reactivity and behavior.
3. How does the hybridization structure of methane and ethane affect their physical properties?
Ans. The hybridization structure of methane and ethane affects their physical properties by influencing their molecular shape and arrangement of electron pairs. This, in turn, affects factors such as boiling points, melting points, and solubility. For example, the tetrahedral arrangement of electron pairs in methane results in a symmetrical molecule with no net dipole moment, making it nonpolar and relatively low in boiling point.
4. Can you explain the concept of sigma bonds in methane and ethane?
Ans. In methane and ethane, sigma bonds are formed between carbon and hydrogen atoms through the overlap of sp3 hybrid orbitals. A sigma bond is a type of covalent bond where the electron density is concentrated along the internuclear axis. These sigma bonds are strong and allow for rotation around the carbon-carbon single bond in ethane.
5. How does the hybridization structure of methane and ethane relate to their reactivity?
Ans. The hybridization structure of methane and ethane influences their reactivity by determining the availability of unpaired electrons for bonding or reaction. The sp3 hybridization in both molecules results in all the valence electrons being paired, making them relatively unreactive compared to molecules with unpaired electrons. However, the sigma bonds in ethane can undergo reactions such as substitution or elimination, leading to the formation of different compounds.
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