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A spacial arrangements of atoms which ca...

A spacial arrangements of atoms which can be converted into one another by rotation arround a C-C single bond are called conformations.
i) Represent Sawhorse and Newman projection formulae of staggered and eclipsed conformation of ethane.

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Draw the Newman projections for staggered and eclipsed conformations of ethane.

A spacial arrangements of atoms which can be converted into one another by rotation arround a C-C single bond are called conformations. ii) Comapare the stabilities of staggered and eclipsed conformations.

Draw the Newman projections of the eclipsed and staggered conformations of ethane molecule.

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Controlled oxidation of alkanes in the presence of suitable catalysts give a variety of products. Free rotation about a carbon - carbon single bond is permitted in an alkane molecule. What are conformers? Draw the structure of the eclipsed and staggered conformers of ethane in Sawhorse and Newman projection and explain their relative stability.

Free rotation is possible with respect to a C-C bond in the case of alkanes. b) Draw Newman's projections of the two conformers of ethane. Which among these is more stable? Justify.

Free rotation is possible with respect to a C-C bond in the case of alkanes. a) The repulsive interaction between the adjacent bonds in a conformation is called…...

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A N EXCEL PUBLICATION-HYDROCARBONS-QUESTION BANK
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  2. Why HCl and HI do not show the peroxide effect?

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  8. The modern theory of aromaticity was advanced by E. Huckel : Give one ...

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  11. Naphthalene is an aromatic compound. Explain its aromaticity using Huc...

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  12. Free rotation is possible with respect to a C-C bond in the case of al...

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  13. Free rotation is possible with respect to a C-C bond in the case of al...

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  14. Free rotation is possible with respect to a C-C bond in the case of al...

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  15. Name the product A.

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  16. Draw the Newman's projections of the eclipsed and staggered conformati...

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  17. What is Baeyer's reagent? Write the chemical equation of its reaction ...

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