![card image](../uploads/69/84/20d22d11_17eb643ad47__8000_00000832.png)
Draw three other possible resonance structures
![card image](../uploads/70/85/20d22d11_17eb643ad47__8000_00000834.png)
![card image](../uploads/71/86/20d22d11_17eb643ad47__8000_00001049.png)
Draw another resonance structures and determine which resonance contributes the most to the resonance hybrid
![card image](../uploads/72/87/20d22d11_17eb643ad47__8000_00001051.png)
The second structure contributes more because the negative charge is on the more electronegative atom (oxygen)
![card image](../uploads/73/88/20d22d11_17eb643ad47__8000_00001053.png)
Determine which resonance structure contributes the most to the hybrid of this structure (out of the three options)
![card image](../uploads/74/89/20d22d11_17eb643ad47__8000_00001055.png)
![card image](../uploads/75/90/20d22d11_17eb643ad47__8000_00001059.png)
Draw a resonance structure that contributes more to the hybrid. Use arrow notations and show all formal charges.
![card image](../uploads/76/91/20d22d11_17eb643ad47__8000_00001061.png)
Draw a Lewis Structure for the following molecule SOCl2 and assign necessary charges.
![card image](../uploads/77/92/20d22d11_17eb643ad47__8000_00001033.png)
Draw a Lewis Structure for the following molecule CH3CH2OCH2CH3 and assign necessary charges.
![card image](../uploads/78/93/20d22d11_17eb643ad47__8000_00001035.png)
Draw a Lewis Structure for the following molecule (CH3)2NNH2 and assign necessary charges.
![card image](../uploads/79/94/20d22d11_17eb643ad47__8000_00001037.png)
Determine the Lewis Structure for acetone (CH3COCH3), Acetic Acid (CH3COOH) and isopropanol ((CH3)2CHOH)
![card image](../uploads/80/95/20d22d11_17eb643ad47__8000_00001063.png)
![card image](../uploads/81/96/20d22d11_17eb643ad47__8000_00001065.png)
Convert the given Lewis Structure of Acetaminophen (Tylenol) into a Condensed Structure
![card image](../uploads/82/97/20d22d11_17eb643ad47__8000_00001067.png)
![card image](../uploads/83/98/20d22d11_17eb643ad47__8000_00001069.png)
For the following compounds, give the chemical formula of the condensed structure
![card image](../uploads/84/0/20d22d11_17eb643ad47__8000_00001071.png)
![card image](../uploads/85/1/20d22d11_17eb643ad47__8000_00001041.png)
Identify the orbitals involved in the labeled carbons:
C1 and H
C2 and O
C3 and S
![card image](../uploads/86/2/20d22d11_17eb643ad47__8000_00001043.png)
![card image](../uploads/87/3/20d22d11_17eb643ad47__8000_00001047.png)
Determine the orbitals for the numbered atoms and bonds:
C1 and adjacent Carbon
N2 and H
C3 and adjacent Carbon
C and S4
![card image](../uploads/88/4/20d22d11_17eb643ad47__8000_00001045.png)
![card image](../uploads/89/5/20d22d11_17eb643ad47__8000_00001075.png)
What is the hybridization and molecular geometry of each labeled atom?
1- sp3 hybridized and tetrahedral
2- sp2 hybridized and trigonal planar
3- sp2 hybridized and trigonal planar
![card image](../uploads/90/6/20d22d11_17eb643ad47__8000_00001077.png)
Rank the following bonds in order of increasing strength
4 < 3 < 1 < 2