Chem/Phys Section Flashcards
(114 cards)
How are amino acids connected to each other and formed into proteins?
The amino terminus of one amino acid attacks the carboxylic-terminal of another.
This is a nucleophilic attack.
What does the interaction of R groups contribute to in the formation of proteins?
Tertiary structure.
The connection of the amino acids contributes to primary structure.
H-bonding between carboxy and amino terminals account for secondary structure such as alpha helices and beta sheets
What amino acid is not optically active?
Glycine because it is the only amino acid without a chiral center
What is a free radical?
An unpaired valence electron.
Nitrile Group
(-CN)
How do we make an electrophile even more electrophilic?
Attach another electron withdrawing group in order to make part of the molecule even more electron deficient so it want the electrons even more.
Grignard Reagent
Grignard reagent is a stronger nucleophile than water. The product of a reaction with Grignard reagent would create new C-C bonds.
Ring Closure of a molecule
Count number of carbons in original molecule! Should match ring. Penultimate OH group acts as the nucleophile that attacks the carbonyl carbon. It is deprotonated and left with an extra pair of electrons.
Carbonyl oxygen turns into another OH group.
Carbonyl is turned into the anomeric carbon in the ring (carbon directly to the right of the O in ring)
Downright Up lefting
Those of Fischer diagram that are on the right point down in the ring and those of Fischer diagram that are on left point up in the ring.
If a D sugar then last group points up in the ring. If an L sugar then last group points down in the ring.
Pyranose
6 membered ring
5 carbons in ring and one Oxygen
Furanose
5 membered ring
4 carbons in ring and one Oxygen
Humans and animals mostly use what kind of sugars?
D sugars
What form of Amino acids is used by cells?
L amino acids. Some D amino acids found in cell walls of bacteria but not in bacterial proteins.
Alpha Anomer in Ring configurations
Alpha anomer points opposite direction of OH to left of O in ring. Alpha anomer is in the axial position.
Fishies are down in the sea
Beta anomer of ring
OH of anomeric carbon is in the equatorial position and points in same direction as the OH group to the left of the O in the ring
Birds are found in the air
Will the material with the lowest index of refraction enable light to travel fastest or slowest?
Lowest index of refraction allows light to travel the fastest
What is myopia and what lens corrects it?
Nearsightedness. Light focuses in front of the retina. Corrected using a concave lens. This lens moves the image back to the retina
What is Hyperopia and how is it treated?
Farsightedness. Object is focused behind the retina. It is treated with a convex (converging) lens
When is the image real for a converging (convex) lens?
Image is real if it placed outside the focal length. Any real image formed by a converging lens is inverted. The retina is small so for it to be possible for it to view an object that is larger than the retina, the formed image must be reduced.
What is etiology?
The cause or set of cause for a disease or condition
What is pathogenesis?
The manner of development of disease
What are anomers?
Anomers differ ONLY in the absolute configuration at their anomeric carbon.
Example is alpha-D-glucose and Beta-D-Glucose.
What are enantiomers?
Enantiomers are mirror images of each other and polarize light oppositely. Example is D-Glucose and L-Glucose
Have SAME physical properties with the exception of direction of polarization of light
What is a reducing sugar?
They are Monosaccharides with a hemiacetal because their open-chain form contains an aldehyde. If the structure lacks any hemiacetal functional groups then it is locked in its cyclic form and is not a reducing sugar.
What is a hemiacetal?
- one OH group and one OR group attached to the same carbon.
- in equilibrium with aldehyde/ketone