Organic Chemistry Special Topics Flashcards

(44 cards)

1
Q

Topics covered

A

Carbohydrates, nucleus acids, amino acids, peptides, proteins, lipids

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2
Q

Carbohydrates

A

Aka saccharides have the general formula of Cn(H2O)m

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3
Q

Sugars

A

Simple carbohydrates

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4
Q

Ketoses

A

Polyhydroxylketones; contain the ketone group

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5
Q

Aldoses

A

Aliphatic Polyhydroxylaldehydes; contain the aldehyde functional group

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6
Q

Monosaccharides

A

Saccharides that cannot be hydrolyzed to simpler structures

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7
Q

Disaccharide

A

Can be hydrolyzed to yield 2 monosaccharides

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8
Q

D or L configuration

A

The configuration of the chiral carbon farthest from the CO group confers to the carbohydrate a sterochemicsl prefix of D or L

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9
Q

Epimers

A

Compounds whose stereochemistry differs at only one carbon

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10
Q

Anomers

A

Diastereomers caused by two possible conformations of a hemiacetal ring

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11
Q

Anomeric carbon

A

The hemiacetal carbon C1

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12
Q

Glycoside

A

Product formed when anomeric carbon reacts with -OH group of an alcohol

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13
Q

Polysaccharide

A

Consist of several monosaccharides liked by glycosidic bonds

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14
Q

Oligosaccharides

A

When polysaccharide contains up to ten monosaccharides

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15
Q

RNA (ribonucleic acid)

A

Contains phosphatesester backbones with two hydroxide on the sugar base

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16
Q

DNA (ddeoxyribonucleic acid)

A

Contains a phosphate water backbone with only one hydroxyl group on the sugar base

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17
Q

Ribonucleosides

A

Building blocks of nucleus acids, which are glycosides of ribofuranose-or ribofuranosides beta, derived from cyclic D-ribose

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18
Q

Pyrimidine

A

Single ring base

19
Q

Purine

A

Two ring base

20
Q

Ribonucleotides

A

When ribonucleosides are phosphorylated at their C5 carbon

21
Q

Four common ribonucleotides

A
Cytidine monophosphate (CMP)
Uridine monophosphate (UMP)
Adenosine monophosphate (AMP)
Guanosine monophosphate (GMP)
22
Q

Four deoxyribonucleosides

A

Deoxycytidine
Deoxythimidine
Deoxyadenosine
Deoxyguanidine

23
Q

Base pairing

A

When bases of DNA hydrogen bond with the other bases

24
Q

Zwitter-ions

A

Diplomat ions like amino acids

25
Isoelectric point
The pH at which the amino acid exists in equilibrium mixture of anionic and cationic forms
26
Peptides
Amino acids linked together
27
Disulfide bridge
Covalent bond formed between two cysteine residues that link together two polypeptide chains
28
N-terminus
First amino acid in the sequence
29
Dalton
A unit of mass equal to the mass of one hydrogen atom
30
Simple proteins
Polypeptide assemblies that hydrolyzed to their constituent amino acid residues
31
Conjugated proteins
Incorporate groups of carbohydrates, lipids, nucleus acids, and various prosthetic groups such as pigments
32
Prosthetic groups
Aka active groups, they are often the site of the main biochemical activity of protein
33
Levels of protein structure
Primary structure Secondary structure Tertiary structure quaternary structure
34
Primary structure
Refer to the covalent assembly or amino acid sequence and the presence of disulfide bridges
35
Secondary structure
Refers to the arrangements adopted by the amino acids sequence; alpha-helix, beta-pleated sheets, random coils
36
Tertiary structure
Represents the complete 3D conformation of the protein and the folding pattern of its secondary structure
37
Quaternary structure
The sum total of the protein assembly, including complication with ligands and inhibitors
38
Simple lipids
Simple hydrocarbon chains that do not hydrolyzed with acidic or basic solvents; terpenes (C5H8)n, steroids, prostaglandins
39
Complex lipids
Are esters of carboxylic acids; they are easy to hydrolyzed to acids and alcohols; include glycerides and waxes
40
Fatty acids
Aka complex lipids; glycerides are the fatty acid seers of glycerol
41
Fats
Triglycerides that are solid at room temperature
42
Oils
Triglycerides that are liquids at room temperature
43
Saturated fatty acid
Fatty acids with no double or triple bonds just plain hydrocarbon chain
44
Unsaturated fatty acids
Fatty acids with double bonds or triple bond in their hydrocarbon chain