Chapter 4 Flashcards
(50 cards)
What is a monosaccharide and what are its types?
Monosaccharides can have 3 carbons (trioses), 4 carbons (tetroses), 5 carbons (pentose), or 6 carbons (hexoses).
What is an aldose? structure of glyceraldehyde? (TEST yourself on structure of glyceraldehyde as well)
An aldose is a carbohydrate that contains an aldehyde group as its highest priority group.
What is a ketose? structure of dihydroxyacetone? (TEST yourself on the structure of dihyroxyacetone)
A ketose is a carbohydrate that containes a ketone group as its highest priority group.
What are Carbohydrates?
Carbohydrates are a class of molecules in the body that consist mostly of carbon, hydrogen, and oxygen.
Test yourself on the structure of D-fructose and its ring!!!!
test yourself
Test your self on the structure of D-glucose!!
test yourself
Test yourself of on the structure of D-galactose
test yourself
Test yourself on the structur of D-Mannose
test yourself
What is a Fischer Projection?
A fischer Projection is a simple two dimensional representation of a three dimensional object in which horizontal lines are wedges coming out at you and verticle lines are dashes going into the page.
What is an enantiomer?
An enantiomer is a molecule with a mirror image exact opposite configuration of the molecule in question. Equal but oposite optical activity
What is a diastereomer?
A diastereomer is a molecule that is not an exact mirror image of the molecule in question, but is still different in its stereochemistry.
What is an epimer?
An epimer is a special type of diastereomers. It is a molecule that is different in configuration at only one carbon. slightly different chemical and physical properties
What is the anomeric carbon?
When a sugar cyclizes, the carbonyl carbon becomes a stereocenter. This is the anomeric carbon.
What types of sugars exist in cyclic form in solution?
Six carbon pyranose rings or five carbon furanose rings.
How do carbohydrates cyclize?
Carbohydrates cyclize by undergoing intramolecular reactions to form cyclic hemiacetals (from aldoses) and hemiketals (from ketoses).
What is a hemiacetal?
A hemiacetal is a product of a hydroxyl group attacking an aldehyde.
What is a hemiketal?
A hemiketal is a product of a hydroxyl group attacking a ketone.
What is an anomer?
An anomer is a molecule that differes in the stereoconfiguration of the anomeric carbon. subtype of epimer
What is meant by alpha and beta anomerism?
Alpha anomeric carbons are trans to the CH2OH substituent, which means they go axial and down. Beta anomeric carbons are cis to the CH2OH substituent, which means they go equatorial and up.
What is a Haworth Projection?
A haworth projection is a 3 dimensional representation of a cyclic sugar.
Represent the sugar with the fischer projection shown below.
Attack the carbonyl (wherever it is) with the last OH on the main chain (on the 5 carbon). Then, all the substituents on the left end up above the ring while all the substituents on the right end up below the ring. The position of the OH on the anomeric carbon is determined by whether or not the molecule is alpha or beta.
What is mutarotation?
When hemiacetal rings are exposed to water, they will spontaneously cycle between the cyclic and the chain form. Because the ring keeps reforming, the anomeric carbon’s alpha or beta designation keeps changing. This spontaneous change in the configuration on the anomeric carbon is known as mutarotation. In glucose beta is favored because alpha has axial OH
What can you do to a solution to increase the rate of mutarotation?
Add acid OR base
What is a reducing sugar?
A reducing sugar is any sugar with a free oxygen on its anomeric carbon or an aldehyde on the end of its chain.
These sugars are so named because they can be oxidized, and are thus considered reducing agents.