B1.1 Carbohydrates and Lipids

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1
Outline the number and type of bonds carbon can form with other atoms.
Carbon can form 4 single covalent bonds
2
Outline the cause and consequence of covalent bonds between atoms
Atoms will covently bond with other atoms for stability by gaining a full shell of electrons
covalent bond formation does not lead to an equal sharing of a pair of electrons between two atoms.
3
Recognize common functional groups.(5)
Hydroxyl,
carbonyl,
carboxyl,
amine,
phosphate
4
List the four major classes of carbon compounds used by living organisms.
Carbohydrates,
lipds,
proteins
, nucleic
acids
5
List example molecules with branched chain
Amylopectin, Glycogen
6
List example molecules with unbranched chain,
Amylose, cellulose
7
List example molecules with single ring
Alpha glucose, beta glucose, ribose, deoxyribose
8
List example molecules with multiple rings
Maltose, sucrose, lactose
9
Define monomer
simple unit that makes up larger molecules
10
Define polymer.
repeating units of monomers
11
Describe condensation reactions
Monomers join together by taking out an OH and an H. Resulting in a loss of a water molecule (H2O).
12
energy from ATP is needed to produce macromolecules by condensation reactions because...
ATP is easily resynthesized in a condensation reaction that adds an inorganic phosphate group to ADP
13
Outline the condensation reactions that form polysaccharides, polypeptides and nucleic acids
Monosaccharide units are joined by a carbon-oxygen linkage known as a glycosidic bond to form a chain called a polysaccharide. When amino acids bond, water is lost and the nitrogen and carbon bond to form a peptide bond, and creates a polypeptide.
14
Describe hydrolysis reactions
chemical reaction where polymer gets broken by water(water breaks bonds) into smallar subunits
15
Outline the hydrolysis reactions that digest polysaccharides, polypeptides and nucleic acids.
A polysaccharide releases energy when digested via a hydrolysis reaction > broken down into monosaccharides.
The hydrolysis reaction of polypeptides breaks them down into monomers that are amino acids
16
Define monosaccharide.
Single sugar molecule,
3-7 carbon atoms
ring structure,
hydrophilic ( soluble in water)
17
Identify pentose and hexose carbohydrates from molecular diagrams.
Pentoses form a 5C ring
hexoses form a 6C ring.
18
Outline the properties of glucose referring to solubility, transportability, stability, and energy yield from oxidation.
Soluble in water,
easily transported through cell membranes,
needed to make ATP during cellular respiration
19
Define polysaccharide.
Polymers of monosaccharides linked by glycosidic bonds to form a chain
20
the structure and function of amylose (starch)
Monomer: Alpha glucose
Branches: no
Helix shape: yes
Glycosidic bond: 1,4
Found in cell type: plant
21
the structure and function of amylopectin(starch)
Monomer:Alpha glucose
Branches: yes(aprox. every 20 monomers)
Helix shape: no
Glycosidic bond: 1,4 + 1,6
Found in cell type: plant
22
the structure and function of glycogen.
Monomer: alpha - glucose
Branches: yes(aprox every 10 monomers)
Helix shape: no
Glycosidic bond: 1,4 + 1,6
Found in cell type: Animal
23
the structure and function of Celluose
Monomer: Beta - glucose
Branches: no
Helix shape: no
Glycosidic bond: 1,4
Found in cell type: plant
24
Discuss the benefit of polysaccharide coiling and branching during polymerization.
Becoming tightly compacted through coiling helps keep energy stored for a later time. In cellulose, it also provides strength in its structure
25
Explain how condensation or hydrolysis of alpha-glucose monomers build or mobilize energy stores
Amylose, Amylopectin, Glycogen, and Cellulose are formed by condensation reactions, polysaccharides release energy via a hydrolysis reaction
26
Define condensation reactions
Polymerization reaction in which two molecules join together
Water is produced
27
Compare the structure of alpha-glucose and beta-glucose.
Alpha glucose has the H above and the OH below the carbon 1, the bond is pointing down
Beta glucose has the OH above and the H below the carbon 1, the bond is pointing up.
28
describe the structure of cellulose microfibrils.protei
bundles of around 36 cellulose chains that are embedded in a matrix of hemicelluloses and lignin.
29
Discuss the consequences of the strength of cellulose in the plant cell wall.
Maintains rigidity strength and shape of cell walls.
30
Outline an example of a function of a glycoprotein.
cell-cell recognition which aids organisation of tissues and allows foreign cells or infected body cells to be identified and destroyed.
31
Compare the structure of the A, B and O glycoproteins on the red blood cell membrane.
A blood type: has A antigens
B blood type: B antigens
AB Blood type: AB antigens
O blood type: lacks antigens that could trigger an immune response(universal donor)
32
Discuss the consequences of the presence of A, B and O glycoproteins during blood transfusion.
If blood transufion has a different type of blood antigen(glycoprotein) than they receptient, the recpitents blood will reject the the blood transfusion and attack the red blood cell
33
Explain why lipids are hydrophobic.
they do not contain a lot of -OH bonds. Instead, they contain a lot of -CH bonds. This causes them to be nonpolar, and not very readily available to form hydrogen bonds with water.
34
Outline the structure and function of oils/triglycerid
3 fatty acids + glycerol, used for long-term energy storage
35
Outline the structure and function of waxe
Composed of long hydrocarbon chains, waxes have a protective and coating function in live organisms as they are insoluble in water and form a waterproof protective coating.
36
Outline the structure and function of steroids.
Have a backbone of four carbon rings, steroids reduce the fluidity of the cell membrane
37
Explain the condensation reaction connecting fatty acids and glycerol to form a triglyceride.
The hydroxyl groups of glycerol combine with the carboxyl groups of 3 fatty acids to form an ester bond
38
Structure and function of phospholipids
Formed by attachment two fatty acids + a phosphate group to a glycerol molecule
39
Explain the condensation reaction connecting fatty acids, glycerol and a phosphate group to form a phospholipid.
The hydroxyl groups of glycerol combine with the carboxyl groups of the fatty acids to form an ester linkage. The third oxygen on glycerol is bonded to phosphoric acid through a phosphate ester bond
40
Describe the structure of a generalized fatty acid.

Long chain of mostly carbon and hydrogen atoms with a COOH carboxyl group at the end
41
Compare and contrast the structures and properties of saturated and unsaturated (mono- or poly-) fatty acids.
Saturated: single bonds in the carbon chain and are solid at room temperature, often from animal sources
Unsaturated mono: 1 doubled bond in the carbon chain, liquid at room temperature, and are often from plant sources.
Unsaturated poly: more than 1 double bond in the carbon chain, liquid at room temperature, and are often from plant sources.
42
Distinguish between the structure and properties of cis- and trans-unsaturated fatty acids.
Cis has hydrogen atoms on the same side of the C double bond and causes a kink in the chain, naturally occuring.

Trans has hydrogen atoms on opposite sides of the C double bond, causes a straighter chain, not found in nature.
43
Outline properties of triglycerides that make them suitable for long-term energy storage.
Triglycerides are excellent long-term energy storage molecules because they will not mix with water and break down.
44
State the function of adipose tissue.
store energy in the form of lipids
45
Discuss the adaptation of a thick adipose tissue layer as a thermal insulator.
It does not transfer heat as well as other tissues and materials—such as muscle or skin, so it is good at insulating and trapping heat.
46
Define hydrophilic, hydrophobic and amphipathic
Hyrdophilic means "water loving,"
hydrophobic means "water fearing,"
amphipathic means having both hydrophilic and hydrophobic part
47
Outline the amphipathic properties of a phospholipid.
A phospholipid has a hydrophilic head and a hydrophobic tail
48
Explain why phospholipids form bilayers in water, with reference to hydrophilic phosphate heads and two hydrophobic hydrocarbon tails.
They form bilayers because of their amphiphilic characteristic. The hydrophilic phosphate heads can bond with water and position themselves on the outside, the hydrophobic hydrocarbon tails do not bond with water so they face away from the water.
49
Structure of steroids
4 carbon rings
17 carbon atoms total in the rings
Hydrophobic
50
State why steroid hormones are able to pass directly through the phospholipid bilayer.
Because they are hydrophobic thus they can easily pass through the phospholipid bilayer
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