![card image](../uploads/1031/44/20d22d11_17eb643ad47__8000_00000504.png)
Label the Bronsted Lowry acid, base, conjugate acid and conjugate base.
![card image](../uploads/1032/45/20d22d11_17eb643ad47__8000_00000506.png)
![card image](../uploads/1033/46/20d22d11_17eb643ad47__8000_00000492.png)
Label the Bronsted Lowry acid, base, conjugate acid and conjugate base.
![card image](../uploads/1034/47/20d22d11_17eb643ad47__8000_00000494.png)
![card image](../uploads/1035/48/20d22d11_17eb643ad47__8000_00000500.png)
Use curved arrow notation to show the movement of electrons in the Lewis Acid-Base Reaction
![card image](../uploads/1036/49/20d22d11_17eb643ad47__8000_00000502.png)
![card image](../uploads/1037/50/20d22d11_17eb643ad47__8000_00000496.png)
Use curved arrow notation to show the movement of electrons in the Bronsted Lowry Acid-Base Reaction
![card image](../uploads/1038/51/20d22d11_17eb643ad47__8000_00000498.png)
![card image](../uploads/1039/52/20d22d11_17eb643ad47__8000_00000560.png)
Label the Bronsted Lowry acid, base, conjugate acid and conjugate base. Then determine in which direction equilibrium is favored.
![card image](../uploads/1040/53/20d22d11_17eb643ad47__8000_00000562.png)
![card image](../uploads/1041/54/20d22d11_17eb643ad47__8000_00000508.png)
Determine in which direction equilibrium is favored.
![card image](../uploads/1042/55/20d22d11_17eb643ad47__8000_00000510.png)
![card image](../uploads/1043/56/20d22d11_17eb643ad47__8000_00000512.png)
Determine in which direction equilibrium is favored.
![card image](../uploads/1044/57/20d22d11_17eb643ad47__8000_00000514.png)
![card image](../uploads/1045/58/20d22d11_17eb643ad47__8000_00000516.png)
Determine in which direction equilibrium is favored.
![card image](../uploads/1046/59/20d22d11_17eb643ad47__8000_00000518.png)
![card image](../uploads/1047/60/20d22d11_17eb643ad47__8000_00000520.png)
Rank the following in order of increasing acidity
![card image](../uploads/1048/61/20d22d11_17eb643ad47__8000_00000522.png)
*Elemental Effect
Electronegativity when comparing CH4, NH3, and CH3OH
Polarizability when comparing CH3OH and HCl
![card image](../uploads/1049/62/20d22d11_17eb643ad47__8000_00000526.png)
Rank the following in order of increasing basicity
![card image](../uploads/1050/63/20d22d11_17eb643ad47__8000_00000524.png)
Negatively charged ions are stronger bases compared to their neutral counterparts
When comparing H2O and NH3, H2O is a stronger acid, because the conjugate base (OH-) is more stable than (NH2-) because oxygen is more electronegative than nitrogen. Since OH- is the more stable conjugate base, it is a stronger acid, and thereby the weakest base.
![card image](../uploads/1051/64/20d22d11_17eb643ad47__8000_00000528.png)
Rank these compounds in order of increasing acidity
![card image](../uploads/1052/65/20d22d11_17eb643ad47__8000_00000530.png)
![card image](../uploads/1053/66/20d22d11_17eb643ad47__8000_00000532.png)
Rank these compounds in order of increasing acidity
![card image](../uploads/1054/67/20d22d11_17eb643ad47__8000_00000536.png)
Elemental Effect (CH3 vs NH2)
Elemental Effect (NH2 vs OH)
Resonance Effect (OH vs. CO2H)
![card image](../uploads/1055/68/20d22d11_17eb643ad47__8000_00000534.png)
Rank these compounds in order of increasing acidity
![card image](../uploads/1056/69/20d22d11_17eb643ad47__8000_00000538.png)
Resonance Effect (OH vs CO2H)
Elemental Effect (CO2H vs HF)
Positively charged ions are stronger acids than neutral counterparts
![card image](../uploads/1057/70/20d22d11_17eb643ad47__8000_00000542.png)
Circle the most acidic proton on each compound
![card image](../uploads/1058/71/20d22d11_17eb643ad47__8000_00000544.png)
A. Inductive Effect
B. Elemental Effect (Eliminates C-H and N-H), (Sulfur is more polarizable than Oxygen)
C. Elemental Effect (Eliminates C-H), Resonance Effect (Eliminates O-H group)
![card image](../uploads/1059/72/20d22d11_17eb643ad47__8000_00000546.png)
Circle the most acidic proton on each compound
![card image](../uploads/1060/73/20d22d11_17eb643ad47__8000_00000550.png)
A. Elemental Effect (Fluorine electronegativity)
B. Hybridization Effect (increase percent s character, closer to the nucleus, more stable)
![card image](../uploads/1061/74/20d22d11_17eb643ad47__8000_00000552.png)
Draw the products for the Lewis Acid and Base Reaction. Identify the electrophile and nucleophile
![card image](../uploads/123/39/20d22d11_17eb643ad47__8000_00001161.png)
![card image](../uploads/1063/76/20d22d11_17eb643ad47__8000_00000556.png)
Draw the products for the Lewis Acid and Base Reaction. Identify the electrophile and nucleophile
![card image](../uploads/124/40/20d22d11_17eb643ad47__8000_00001165.png)