Chapter 2.3: Organic Compounds Flashcards

(40 cards)

1
Q

Organic Compounds

A

Chemicals produced by living organisms.

Much larger & complex than inorganic.

Has a CARBON-HYDROGEN BACKBONE, with the addition of groups of atoms called functional groups.

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

Hydrocarbons

A

Organic compounds that contain only hydrogen & carbon.

Can exist as CHAINS or RINGS

Carbon is in the middle if the chain, or the center of the ring.

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

Monomers & Polymers

A

Single subunits that can be combined to build larger structures.

Larger structures consisting of many monomers.

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

Dehydration Synthesis

A

Polymers that are built by an ANABOLIC REACTION, in which two monomers are linked by a COVALENT BOND.

The products of dehydration synthesis are a polymer compound and a molecule of h2o.

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

Hydrolysis

A

A CATABOLIC PROCESS in which a molecule of h2o is added to the polymer, the atoms in the h2o molecule split apart, and the covalent bonds between monomers are broken.

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

Carbohydrates

A

Only accounts for 1% of the body’s mass and have few structural roles.

Monomers of carbohydrates are composed of:

Carbon: 1
Hydrogen: 2
Oxygen: 1

=Two hydrogen atoms for every carbon & oxygen atom

*Because carbs contain several -OH (hydroxyl groups), the compounds are POLAR & HYDROPHILIC.

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

Monosaccharide

A

The monomer of Carbohydrates.

Has 3 to 7 carbon atoms

Generally RING STRUCTURE

Majority in body have:

5 carbons: pentoses

6 carbons: hexoses

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

The primary pentose sugars

A

Ribose: c5-h10-o5 (2:1 ratio)

Deoxyribose: c5-h10-o4

(loss of one oxygen, so deoxy)

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

Primary hexose sugar

A

Glucose: c6-h12-o6

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

Two other major hexoses

A

Isomers of glucose:

same molecular formula, but DIFFERENT STRUCTURE.

Fructose: c6-h12-o6

Galactose: c6-h12-o6

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

Disaccharide

A

A compound w/ two monosaccharides joined by a POLAR covalent bond.

Formed by dehydration synthesis:

Glucose (remove -OH)+ Fructose (remove H) = Sucrose

Can be broken down into monosaccharides by hydrolysis.

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

Polysaccaharides

A

Polymers composed of long, branching chains of monosaccharides.

The monosaccharides are joined by covalent bonds formed by dehydration synthesis.

*Polysaccharides are not very soluble in h2o, even-though they are composed of polar/ hydrophilic monomers. -Mostly due to size b/c large compounds are difficult for h2o molecules to separate from one another, regardless of polarity

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

Glycogen

A

The polysaccharide storage form of glucose, found in the liver & skeletal muscles.

Ideal b/c complex str. and low-solubility enhances storage ability.

Branched ends allow enzymes many ends from which to catalyze hydrolysis reactions, so blood glucose can be increased quickly.

Exhausted in about 2hrs. before the liver & muscles need new glucose molecules.

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

Glycoproteins & Glycolipids

A

Carbs that are attached to proteins & lipids by covalent bonds.

They help maintain cell structural integrity & enable cells to recognize & communicate (Cell-Cell Communication Core Principle)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q
A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Lipids: composition & characteristics

A

Mainly composed of Carbon & Hydrogen (c15-h31-COOH)

Because Lipids are predominately composed of C-H, they are non-polar & hydrophobic.

Lipids will dissolve in, or act as a solvent for other non-polar compounds (lipid-soluble)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Fatty Acid

A

A basic lipid monomer.

Structure is a hydrocarbon chain w/ 4 to 20 plus carbon atoms bonded to a carboxylic acid group (—COOH).

18
Q

Saturated Fatty Acid

A

No double bonds between carbon atoms in its hydrocarbon chain, so its carbon atoms are “saturated” with H atoms.

-Animal fats. Solid at room temp.

19
Q

Monounsaturated FA

A

One double bond between two carbons in its hydrocarbon chain.

-Melts at room temp.

-Olive oil

20
Q

Polyunsaturated FA

A

Two or more double bonds between its carbon atoms.

-Lowest melting point of all FAs. Def liquid at room temp.

21
Q

Glycerol: how the body stores FAs

A

FAs cannot be packaged into long chains like monosaccharides.

So the body links 3 FAs via dehydration synthesis to a modified three-carbon sugar known as: GLYCEROL.

Glycerol plus the 3 FAs are Triglycerides

22
Q

Triglyceride

A

A polymer composed of glycerol plus 3 FA chains that are joined by dehydration synthesis.

Aka- Neutral Fat

If one or more of the 3 FA chains are unsaturated, it is likely to be liquid.

23
Q

Phospholipid

A

Similar structure to Triglyceride, with a glycerol backbone, but with only 2 FA chains (non-polar) plus a Phosphate group (polar).

This compound is amphiphilic, in that it has both polar & non-polar parts.

24
Q

Steroids/ Sterols

A

Lipids that have a four-ring hydrocarbon structure (steroid nucleus).

Cholesterol forms the basis for the body’s’ other steroids.

25
Protein: function & structure
Proteins are macromolecules that act as enzymes, have structural roles, allow cells to communicate, make muscle contraction & can be oxidized for fuel. The monomer of all proteins are Amino Acids.
26
Amino Acids
Monomer of all proteins. A central Carbon atom Bonded to 4 chemical groups; The nitrogen-containing AMINO GROUP (—NH2) plus the CARBOXYLIC ACID GROUP A hydrogen atom An atom or atoms of the “R” group (“residue”)
27
28
R group in proteins
R group determines the AAs properties Range from one simple H atom, to complex. Can act as a acid/base, polar/nonpolar Determines proteins behavior in h2o
29
Peptide & Peptide Bonds
AA monomers can be linked by dehydration synthesis to form polymers. Can be reversed thru hydrolysis. Two AA joined by a polar covalent bond, which are PEPTIDE BONDS. Polypeptides = 10 or more AAs
30
Fibrous protein
Long protein strands composed of mostly non-polar AAs, resembling ropes that “tie” the body’s structures together. Found in hair, nails, tendons & bone
31
Globular proteins
Polypeptide chains that assemble into a globe that are mostly polar. Enzymes, hormones & other cell-messengers.
32
4 levels of protein structures
1. Primary: AAs in a linear polypeptide held together by covalent peptide bonds. 2. Secondary: Folding patterns of alpha helix (spring like), beta pleated sheets (vertical blinds) 3. Tertiary The final 3d shape that makes the protein FUNCTIONAL. H bonds, covalent bonds & ionic interactions between R groups. The IONIC INTERACTIONS BETWEEN R-GROUPS HELP TO DETERMINE THE SHAPE THE PROTEIN ASSUMES AFTER IT IS FOLDED. (2nd & 3rd shapes are almost identical in fibrous proteins) 4. Quaternary: Assembled polypeptide chains consisting of of their own primary, secondary & tertiary shape.
33
Nucleotide & Nucleic Acids
-Nucleotides are monomers that form our genetic material & also ATP. (Nucleotide= Nitrogenous base + Pentose sugar+ Phosphate group) -Nucleic Acids are polymers of linked nucleotides. (Ex. DNA & RNA.) The nucleotides are joined by dehydration synthesis: the phosphate group of one nucleotide is joined to the sugar of the next by a polar covalent bond. Nucleic Acids are Not oxidized for fuel, but nucleotide ATP is.
34
Nucleotide Structure: 3 parts
1.) Nitrogenous base + (glycosidic bond w/ the “1” Carbon of the sugar) 2.) A five-carbon (pentose) sugar + (covalent bond) 3.) A phosphate group
35
Nitrogenous base: 2 types involved in DNA/RNA
A nitrogen containing hydrocarbon ring structure. Purines: double-ringed compounds include bases ADENINE & GUANINE Pyrimidines: single-ringed compounds including bases Cytosine, Thymine & Uracil. Known as: A-G-C-T-U
36
Pentose-sugar in Nucleotides
A five-carbon sugar, Ribose or Deoxyribose sugar. Covalently bonded to a phosphate group. Nucleotides can contain between 1 to 3 groups.
37
ATP
A nucleotide that is the main source of chemical energy in the body. Adenine + Ribose = Adenosine Plus 3 Phosphate groups
38
ATP synthesis from ADP
Generally accomplished by adding a 3rd phosphate group. This is a highly endergonic reaction due to the energy needed to overcome the negative charges on the phosphate groups. However, when the phosphate bond is broken thru hydrolysis, the reaction is highly exergonic b/c ADP is more stable than ATP.
39
DNA function & characteristics
DNA is an extremely large polymer found in the nucleus. Its function is the genetic code, the specifications of AA sequence for each protein. Cells read this sequence & assemble proteins via protein synthesis. Composed of two long chains of nucleotides that use H bonds to form a double-helix. Contains the pentose sugar, Deoxyribose (“de” because one of its carbon atoms lacks a hydroxyl group (-OH) and instead just has a H atom. Contains only bases: AGCT Complimentary base pairing determined by number of H bonds: A (purine) & T (pyrimidine) [2 H bds] G (purine) & C (pyrimidine) [3 H bds]
40
RNA function & characteristics
DNA is not directly involved in the assembly of proteins involved in protein synthesis. DNA= contains instruction for building every protein in the body RNA= carries out DNA’s instruction Rather, RNA actually assembles the correct AA sequence for a protein. Consists of a single strand of nucleotides and is not confined to the nucleus. Must be able to travel to carry out genetic code & assist with transcription & translation. Structure: Pentose sugar Ribose Plus Nitrogenous base Uracil instead of Thymine. Pairings: U & A C & G (When RNA bonds to another nucleotide strand)