3.1 carbon and the molecular diversity of life and functional groups Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

organic chemistry defintion

A

branch of chemistry that specializes in study of carbon compounds

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

organic compounds contain what elements?

A

carbon and hydrogen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what are the major elements of life?

A

carbon
hydrogen
nitrogen
oxygen
phosphorous
sulfur

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

how many valence electrons does carbon have?

A

4 (tetravalence)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

how many bonds can carbon form?

A

up to 4

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what are carbon’s most frequent bonding partners?

A

hydrogen
oxygen
nitrogen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

alkane

A

single bond

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

alkene

A

double bond

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

alkyne

A

triple bond

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what are the 4 classes of macromolecules?

A

carbohydrates
proteins
lipids
nucleic acids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what 3 shapes can carbon molecules form?

A

chains
ring-shaped
branched

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

isomer definition

A

molecules have the same molecular formula, differs in atom arrangement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

different molecule structure =

A

different properties and functions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

structural isomer

A

varies in covalent arrangement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

cis-trans isomer

A

differs in spatial arrangement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

enantiomers

A

mirror images of molecules

17
Q

most common functional groups

A

hydroxyl
carbonyl
carboxyl
amino
sulfhydryl
phosphate
methyl

18
Q

hydroxyl structure

A

–OH
(or HO–)

19
Q

hydroxyl name of compound

A

alcohols (specific names end in -ol)

20
Q

hydroxyl functional properties

A

polar, results from electrons spending more time near electronegative oxygen atom

can form hydrogen bonds with water molecules, helping dissolve organic compounds such as sugars

21
Q

carbonyl structure

A

> CO

22
Q

carbonyl name of compound

A

ketones if carbonyl group is within a carbon skeleton

aldehydes if carbonyl group is at the end of the carbon skeleton

23
Q

carbonyl functional properties

A

ketone and aldehyde might be structural isomers with different properties, similar to acetone and propanal

ketone and aldehyde groups are also found in sugars, giving rise to to major groups of sugars: ketoses (containing ketone groups) and aldoses (containing aldehyde groups)

24
Q

carboxyl structure

A

–COOH

25
Q

carboxyl name of compound

A

carboxylic acids, or organic acids

26
Q

carboxyl functional properties

A

acts as an acid, can donate an H+ because the covalent bond between O and H is so polar

found in cells in the ionized form with the charge of 1- and called a carboxylate ion

27
Q

amino structure

A

–NH2

28
Q

amino name of compound

A

amines

29
Q

amino functional properties

A

acts as a base, can pick up an H+ from the surrounding solution (water, in living organisms)

found in cells in the ionized form with a 1+ charge

30
Q

sulfhydryl structure

A

–SH

31
Q

sulfhydryl name of compound

A

thiols

32
Q

sulfhydryl functional properties

A

two sulfhydryl groups can react, forming a covalent bond. cross-linking helps stabilize protein structure

cross-linking of cysteines in hair proteins maintains the curliness or straightness of hair. straight hair can be permanently curled by shaping it around curlers and then breaking and re-forming the cross-linking bonds

33
Q

phosphate structure

A

–OPO3^2-
–OPO3H2

34
Q

phosphate name of compound

A

organic phosphates

35
Q

phosphate functional properties

A

contributes negative charge to the molecule of which it is a part (2– when at the end of a molecule, 1– when located internally in a chain of phosphates)

molecules with phosphate groups have potential to react with water, releasing energy

36
Q

methyl structure

A

–CH3

37
Q

methyl name of compound

A

methylated compounds

38
Q

methyl functional properties

A

addition of a methyl group to DNA, or to molecules bound to DNA, affects the expression of genes

arrangement of methyl groups in male and female sex hormones affects their shape and function