Review 1 Flashcards
3 Indicators and their Range
- Methyl Red = 4.4 - 6.2
- Bromothymol Blue = 6 - 7.6
- Phenolphthalein = 8.2 - 10
Two Methods for Alpha amino acid Synthesis
- Gabriel Synthesis
2. Strecker Synthesis
Gabriel Synthesis
N-pthalimidomalonic acid (2 COOEt (One for COOH and the other to activate COOH and N-bound to aromate for Amino Group) -> Alkylated to add R group (use base and R-X) -> Acid-hydrolysis (to add Nitro and carboxy on both siddes) -> Heat to form the alpha-amino acid and addition of H and removal of one of the COOH
Strecker Synthesis
- Aldehyde or Ketone acts as the backbone for amino acid
- :NH3 = Precursor for amino group
- KCN = Precursor for Carboxy group
Strecker Synthesis Process
Aldehyde or Ketone + :NH3 -> Water and Imine
Imine with Acid and KCN -> Alpha amino nitrile + acid -> amino acid
Transport Proteins
The higher the concentration of the ligand, the higher the binding affinity while the lower the concentration of the ligand, the lower the binding affinity
Purines
Adenine and Guanine
Pyrimidines
Cytosine and Thymine
Difference between Purines and Pyrimidines
Purines have a double ring structure and Pyrimidines hae a single ring structure
Why is DNA called an acid even with Nitrogenous bases
They have phosphate groups that are usually protonated but remain deprotonated in the solvent.
Saponification
Base-Catalyzed Ester hydrolysis of triglycerols that lead to polar and non-polar sides for soaps to function. This is the process by which fats are metabolized.
Types of Lipids
Hydrolyzable and Non-hydrolyzable lipids
4 examples of hydrolyzable Lipids
- Triglycerols - Saponification
- Phospholipids - Hydrolyzable because of phosphate
- Sphingolipids - Sphingosine + substituting OH for phosphate
- Waxes - Hydrolyzable because of the C=O
1 = Energy storage and 2 = Structural function
3 examples of non-hydrolyzable lipids
- Prostagladins - Inflammation signalling molecule
- Steroids - 6-6-6-4 rings with differing substituents for structural purposes
- Vitamins - Cofactors
a. A - Retinol (light sensitivity)
b. D - Bones (Rickets and Osteoporasis)
c. E - Antioxidant (protects neurological function)
d. K - Prothrombin (blood clot)
Effect of Common ion on Solubility
Common ione effect decreases solubility and shifts the equilibrium to the left as a result of Le Chatelier’s principles
Effect of pH on solubility
If the salt dissociating has a strong conjugate base, it will combine with the proton and form an acid and water. Note it does not work on all salts because the stronger the acid, the weaker the conjugate base. For example:
CaF2, F- will combine with H+ to form a weak acid but AgCl2 will not form an acid because it has a weak conjugate base and strong acid.
Effect on equilibrium of solubility from pH
The proton reacts with the specific ion and takes it out of solution, this will shift the equilibrium to the right to relieve the stress
Effect of dissolving NH3 and AgCl2
This will lead to the dissolution of AgCl2 into Ag 2+ and Cl-, the Ag 2+ will combine with NH3 to form a complex ion which is highly favorable. The overall effect is that more of AgCl2 will dissolve because the equilibrium shifts to the right
Acid/base NH3 and AgCl2 explanation
NH3 acts as a Lewis base (electron pair donor) and Ag2+ acts as a Lewis acid (electron pair acceptor)
CASHNGIA Explanation
C - Chlorates A - Acetates S - Sulfates H - Halides N - Nitrates G & I - Group I metals A - Ammonium