Answer the following questions about the cyclopropenyl anion: a. How many T-electrons does the compound have? b. Draw the molecular orbital (MO) energy diagram for the cyclopropenyl anion. You must label the bonding and antibonding orbitals and place the r-electrons in the orbitals. (You do not need to draw pictures of the orbitals, just arrange the energy levels.) c. Is cyclopropenyl anion aromatic, antiaromatic or nonaromatic? Explain by referring to your MO diagram.

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter14: Conjugated Compounds And Ultraviolet Spectroscopy
Section14.SE: Something Extra
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Organic Chemistry Question 

PLEASE SHOW STEP BY STEP, WITH ARROWS! ALSO PLEASE INCLUDE ALL ELECTRON LONE PAIRS AND CHARGES FOR STRUCTURES IF NECESSARY!

Answer the following questions about the cyclopropenyl anion:
a. How many T-electrons does the compound have?
b. Draw the molecular orbital (MO) energy diagram for the cyclopropenyl anion. You must label
the bonding and antibonding orbitals and place the n-electrons in the orbitals. (You do not need
to draw pictures of the orbitals, just arrange the energy levels.)
c. Is cyclopropenyl anion aromatic, antiaromatic or nonaromatic? Explain by referring to your MO
diagram.
Transcribed Image Text:Answer the following questions about the cyclopropenyl anion: a. How many T-electrons does the compound have? b. Draw the molecular orbital (MO) energy diagram for the cyclopropenyl anion. You must label the bonding and antibonding orbitals and place the n-electrons in the orbitals. (You do not need to draw pictures of the orbitals, just arrange the energy levels.) c. Is cyclopropenyl anion aromatic, antiaromatic or nonaromatic? Explain by referring to your MO diagram.
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