Some random stuff I wrote down on my notes as I was studying for the MCAT. Thought I'd share with you guys. Highlight the area below the question for the answer. Feel free to add
Unsaturation in alkene increases or decreases viscosity?
Decreases
Difference between regioselectivity and stereoselectivity?
For example, hydrogenation of alkene via H2/Ni is stereoselective but not regioselective. Since hydrogenation is cis, it's stereoselective. But since both carbons receive hydrogens, it's not regioselective.
Adding dielectric stuff between the capacitor plates increases or decreases the capacitance?
Increases
Iodoform reaction (I2/Oh-) tests for what functional group?
Methyl Ketone
Solubility: Cl-, Br-, I- ions are soluble except for?
Ag+, Hg2++, Pb++
What happens to carbonyl in Wittig reaction?
C=O bond is replaced with C=CRR' bond
Naturally occurring amino acids are L or D?
L
Naturally digestible sugars are usually L or D?
D
Wolff-Kishner reduction (reagent N2H4) does what to carbonyl?
Replaces C=O bond with two C-H bonds
Unsaturation in alkene increases or decreases viscosity?
Decreases
Difference between regioselectivity and stereoselectivity?
For example, hydrogenation of alkene via H2/Ni is stereoselective but not regioselective. Since hydrogenation is cis, it's stereoselective. But since both carbons receive hydrogens, it's not regioselective.
Adding dielectric stuff between the capacitor plates increases or decreases the capacitance?
Increases
Iodoform reaction (I2/Oh-) tests for what functional group?
Methyl Ketone
Solubility: Cl-, Br-, I- ions are soluble except for?
Ag+, Hg2++, Pb++
What happens to carbonyl in Wittig reaction?
C=O bond is replaced with C=CRR' bond
Naturally occurring amino acids are L or D?
L
Naturally digestible sugars are usually L or D?
D
Wolff-Kishner reduction (reagent N2H4) does what to carbonyl?
Replaces C=O bond with two C-H bonds
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