Axial Position
What is the difference between axial and equatorial position in molecules?
[2008-12-06 12:38:32]

Q:

A: Imagine the world. Take your center object in the middle of the earth. Now your equatorial atoms are those at the equator and your atoms would axial north and south pole.

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Chemistry »

n a trigonal bypyramidal molec, why does a lone pair occupy an equatorial position rather than axial position?
[2009-04-19 21:29:11]



The lone pair repels other electrons slightly more than bonding electrons repel other electrons. You can think of the lone pair as being slightly bigger. Since the axial electrons are more crowded, a lone pair on the axial position would have a slightly

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My own background is in political philosophy and the history of political thought: so that naturally informs my own reactions as do my political engagements and sympathies. Begins with a conversation in a London churchyard about debt and morality and takes us all the way from ancient Sumeria,......

Chemistry »

Why are some axial functional groups on Cyclohexane lower in energy compared to equatorial position?
[2008-10-02 15:11:33]

I was using Spartan and we needed to build some molecules and see if was saw any interesting properties.

I came across building Cyclohexane with a cyanide functional group attach to it (sorry I haven't learned the proper naming system yet)


The cyano substituent in the axial position produces approx 0.4kJ/mol per 1,3-diaxial interaction, so the total strain the program should display is 0.8kJ/mol, while the equatorial position has zero strain. Make sure the ring flipped cyclohexanecarbonitrile

Chemistry »

Cis-1,3-dimethylcyclohexane, with CH3 in axial position. Do ring flips and examine the 2 chair conformations?
[2008-09-30 13:49:07]

which is more stable?

2) Trans-1,3-dimethylcylohexane with CH3 group axial and the other equatorial, do ring flips and examine the 2 chair conformations, which is more stable? Given the 2 isomers, trans 1,3-dimethylcyclohexane and cis-1,3-dimethlcyclohexane,