Practice Exam 1 Flashcards
Sn1 reactions
Tertiary alcohols, carbocation and varied stereochemistry. 2 products
Sn2 reactions
Primary and Secondary alcohols, INVERTED stereochemistry and only 1 product
Chromatography TLC and Paper
TLC- gel Paper-celullose Stationary phase is more polar If water is stationary phase then since you know water has hydrogen bonding the mobile phase that “sticks” the most to the stationary phase will be the one with more hydrogen bonding. Also, if more polar sticks more. Non polar travel further
Gas chromatography
Smallest molecular weight and weakest intermolecular forces will travel the fastest
Forming an Ester Who loses OH
Ester: COOH + ROH Carboxylic Acid loses OH
Enzymes affect chemical reactions by stabilization of
the transition state changes the activation energy of the reaction
To decrease the ionization of CH3COOH (acetic acid) [weak acid btw]
Add a strong acid like HCl, which will increase the H+ in solution and decrease the amount of CH3CO2H that ionizes
Strong acids
HCLO4 perchloric acid HCl, HBr, HI H2SO4 HNO3
Einstein-Plank Equation
E= h*f= h*c/lambda
Standard Atmospheric Pressure
760mmHg
9L/ 10 min
9000ml/10 min—> 900/min
Peptide bonds
Planar bond, can have double bond character due to resonance
Peptide Bond
N—–C Lose a water molecule when forming a peptide bond
AA abreviations Asp Asn Arg
Aspartic Acid (Acid) Asparginine (3N’s) Arginine (basic)
What is special about the side-chains of aa?
Their net charge responds to pH
Octohedral compounds
d2sp3
Ideal gas
Intermolecular forces and individual volume are negligible