Focus 2.57


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Jessica Luong 3K
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Joined: Sat Aug 17, 2019 12:17 am

Focus 2.57

Postby Jessica Luong 3K » Sun Nov 24, 2019 11:24 pm

Acetonitrile, CH3CN, is used as a solvent in the pharmaceu- tical industry. Describe the structure of the CH3CN molecule in terms of hybrid orbitals, bond angles, and s- and p-bonds. The N atom is a terminal atom.

Alexis Webb 2B
Posts: 124
Joined: Thu Jul 11, 2019 12:15 am

Re: Focus 2.57

Postby Alexis Webb 2B » Mon Nov 25, 2019 2:47 pm

When you draw out the Lewis structure, there will be a tetrahedral shape around one C atom and a linear shape on the other C atom. Then, you can determine the bond angles. For hybrid orbitals, you think about the number of bonding regions around the central atom you have. For tetrahedral, there are four, so it would be sp3. For linear, there are two bonding regions, so it would just be sp.
Last edited by Alexis Webb 2B on Tue Nov 26, 2019 5:12 pm, edited 1 time in total.

LBacker_2E
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Re: Focus 2.57

Postby LBacker_2E » Tue Nov 26, 2019 9:50 am

I'm confused, is this question asking you to write out the hybridizations for each sigma and pi bond like in 2.47 or is it asking for the hybridizations of the central atoms?

Alexis Webb 2B
Posts: 124
Joined: Thu Jul 11, 2019 12:15 am

Re: Focus 2.57

Postby Alexis Webb 2B » Tue Nov 26, 2019 5:13 pm

It is asking for the hybrid orbitals for the central atoms.

NRodgers_1C
Posts: 54
Joined: Thu Jul 25, 2019 12:15 am

Re: Focus 2.57

Postby NRodgers_1C » Sat Nov 30, 2019 6:27 pm

For this problem, I just drew out the Lewis structure then counted the regions of electron density on each central atom (both Carbons and the Nitrogen) to determine the hybrid orbitals. From there, I just used my knowledge of bond angles in relation to the VSEPR geometries and number of bonds to determine the bond angles and σ- and π-bonds.


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