QUIZ 2 Flashcards

1
Q

What is a polymer?

A

Long chains of repeating subunits,

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2
Q

What are ANABOLIC reactions?

A
  • they require the use of energy to build larger molecules from small subunits

EX: Condensation Reaction / Dehydration Synthesis

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3
Q

What are CATABOLIC reactions?

A
  • they release energy by breaking large polymers into shorter polymers

EX: Hydrolysis Reactions

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4
Q

What are CARBOHYDRATES?

A
  • sugar molecules
  • made of carbon, hydrogen, oxygen
  • monomer = monosaccharide
  • Monosaccharide = a group of carbohydrates made only of a single saccharide; single sugar
    —> they are linear in dry state, ring structure when dissolved in water
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5
Q

What are the three monomers for carbohydrates (monosaccharides)?

A

1) Glucose (OH BOTTOM of C4)
2) Fructose (Pentagon shape)
3) Galactose (OH TOP of C4)

NOTE: carbon 1 is directly after O bond, alpha = OH BOTTOM of C1, beta = OH TOP of C1

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6
Q

What is a DISACCHARIDE?

A
  • group of carbohydrates made of two monosaccharides linking together; double sugar
  • Sugars joined by condensation/dehydration synthesis –> make glycosidic linkages (covalent) b/w hydroxyl groups
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7
Q

What is a POLYSACCHARIDE?

A
  • 3 or more sugars joined by glycosidic linkages between hydroxyl groups

1) Glycogen (storage for animals)
2) Starch (storage molecule for plants)
3) Cellulose (structural polysaccharide for plants)
4) Chitin (structural polysaccharide)
*ALL polymers of GLUCOSE

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8
Q

STRUCTURAL vs STORAGE

A

Storage: same direction bonds, plant storage entirley of glucose
strucutral: bonds going in different directions, Glucose cant break bonds, made up of beta glucose

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9
Q

What are the NUCLEIC ACIDS?

A

1) DNA (deoxyribonucleic acid) H on seconds carbon
2) RNA (ribonucleic acid) OH on second carbon

  • monomer = nucleotide subunits
    –> a sugar, base and phosphate
  • allow for reproduction
  • store hereditary information that determines structural and functional characteristics
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10
Q

What are the 2 types of NITROGENOUS BASES?

A

1) Pyrimidine bases: single organic rings (ex. uracil, thymine, cytosine)

2) Purine bases: two-ringed organic structures. (ex. adenine, guanine)

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11
Q

How do you form DNA/RNA?

A
  • chains of nucleotides –> one nucleotide linked to the next by a single bridging phosphate group between C5 of one sugar and C3 of the next sugar in line
  • forms PHOSPHODIESTER BONDS
  • condensation/dehydration synthesis reaction
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12
Q

DNA vs RNA

A

DNA
- composed of two strands wound around each other in a double helix and held together by hydrogen bonds
- Adenine, Guanine, Thymine, Cytosine
- Deoxyribose -H

RNA
- single strand of nucleotides
- Adenine, Guanine, Uracil, Cytosine
- Ribose -OH group

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13
Q

Hydroxyl Alcohols/sugars

A

Group: HYDROXYL
Name of Compound: Alcohols/sugars
Draw
Behaviour: Polar O-H, interacts strongly with water
ends in ol ex: ethanol

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14
Q

Methyl Hydrocarbons

A

Group: METHYL
Name of Compound: Hydrocarbons, oils
Draw
Behaviour: Non polar C-H bonds, doesnt interact with water well
C with 3 H

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15
Q

Carbonyl Aldehyde, ketons

A

Group: CARBONYL
Name of Compound: Aldehydes/Ketones
Behaviour:
1) Aldehyde- polar H-C=O interacts with water highly reactive
2) Ketones- polar C=O interacts with water somewhat reactive

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16
Q

Carboxyl organic acids

A

Group: CARBOXYL
Name of Compound: Organic Acids
Behaviour: COOH when donating water to increase acidity dissociates to COO (-) interacts strongly with water (gives H+ ions)

17
Q

Amino Organic bases

A

Group: AMINO
Name of compound: Organic Bases
Behaviour: NH3 acts as base and interacts with water H-N-H (takes H+ ions)

18
Q

Phohphate organci phosphates

A

Group: PHOSPHATE
Name of Compound: Organic Phosphates
Behaviour: release two protons H2PO4–> PO4 2-linked to form di and tri phosphates O–P-O-O, strong reaction with H2O

19
Q

Sulfhydryl Thiols

A

Group: SULFHYDRYL
Name of compound: Thiols
Behaviour: resembles Oh group in shape O–C-OH , CH2-SH, H-N-H

20
Q

Macromolecules

A

Large molecules that are sometimes composed of a great number of repeating subunits

21
Q

What are Lipids and how are they formed

A
  • Fats, most common storage molecule, composed of carbon, hydrogen and oxygen
  • formation: Hydrocarbon link together to form long chains that can vary 12- 24 carbons in length
  • Hydrophobic bc more non polar C-H bonds and less polar than O-H bonds
    Insolubility contributes to ability to form cell membranes
  • Groups: fatty acids, glycerides, phosolipids
22
Q

Fatty acids

A
  • long carbon chain with carboxyl group COOH gives it its acidic properties
  • can be saturated and unsaturated
  • Saturated: Has the max amount of H, heart disease and high cholesterol
  • Unsaturated: Kink, has a double bond, not max # of H because of a double bond, helps clean blood vessels
23
Q

Glycerides

A
  • Fatty acids that join together to form a glycerol backbone through condesation reactions bw carboxyl group of the fatty acid and the hydroxyl group of the glycerol forming and ester linkage
  • Condensation Takes out the waters and creates and ester linkage and water as a byproduct
  • Hydrolysis breaks that ester linkage by adding the same amount of waters as bonds to make two smaller molecules (breaking down tryglyceride)
24
Q

Phospholipids function and what they are

A
  • Glycerol with 2 fatty acids and a phosphate group attached to the glycerol backbone
  • Fatty acids (tails) are hydrophobic (non polar)
  • phosphate group (head) are hydrophilic (polar)
    Function: form double layer-> forms cell membranes
  • functional cell membranes contain proteins and hydrophilic pores that form channels through charged materials can pass
25
Waxes
- long fatty acid chains linked to alcs or carbon rings Function: - Waterproof coatings (ex leaves, feathers) - helps plants conserve water and also acts as a barrier to infection - waxy coating holds water in but also acts as a barrier
26
Steroids
- 4 fused carbon rings with several functionnel groups Function: - Cholesterol adds rigidity to membranes - importants component to cell membranes - in medicine are used to reduce inflammation - Hormones
27
Proteins
- Polymers of amino acids - monomer= amino acid - Most diverse
28
Amino acids
- 20 different - Backbone: One central carbon atom, amino group, carboxylic acid group - Radical/side group gives the amino acids their individual properties Formation: Amino acids join by dehydration to form dipeptides and polypeptides with peptide bonds C-N --> hydrolysis to break down
29
Strucuture steps of proteins first 2
1) Primary: Linking arms, sequence of aminos, held together by peptide bonds 2) Secondary: Folding creating H bonds, can fold differentley alpha: helix h bonds bw the nitrogen of amino, Beta: pleated sheets, H bonds bw diff polypeptides chains
30
Structure steps of protein last 2
3) Tertiary: Fold further, stabilized by R groups interactions, 3-dimensional 4) Quaternary: Clustering of two or more polypeptides, Proteins need to be in their ideal environment to fold properly - bonds cant refold when in stage one and will become denatured
31
Proteins shape
- conformation - if protein loses its conformation it is denatured due to pH, salt concentration, temp - loss in shape = loss of function