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Explain following question ❓
For the given compound (I), the possible conformations are shown by (III) and (IV). Form the III and IV, III is more stable than the IV because the larger group, ethyl, is at an equatorial position.
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- Which has the greater polarizability? Explain.(a) Br⁻ or I⁻ (b) CH₂=CH₂ or CH₃—CH₃(c) H₂O or H₂SeArrange the following in increasing order of boiling point:(i) CH3CH2CH2CH2Br(ii) (CH3)3.Br(iii) (CH3)2C.BrArrange the following in increasing order of boiling point: (i) CH3CH2CH2CH2Br(ii) (CH3)3Br(iii) (CH3)2CBr
- Perspective drawings of Chair and Boat Conformers fo Cyclohexane (C6H12). Note it is impossible to place all the carbons in the same plane without straining the bonds. Take two opposite carbons and pull both of them up to make one conformation adn then pull one of them down to make the other conformation. Can you inercovert one conformer int othe other without breaking any bonds? Explain why these represent conformers and not isomers.Do ethanol (C2H5OH) C and DDraw 2 isomenthol chair conformers. Include axial and equatorial groups. Explain which is more stable.