BIO SEM 1 UNIT 4

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Last updated 9:22 PM on 6/22/26
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30 Terms

1
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What elements are organic molecules built from, and name the major classes of biomolecules.

Carbon plus a few other atoms (commonly H, O, N, P, S); major biomolecule classes are nucleic acids, proteins, carbohydrates, and lipids

2
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What two features of carbon give organic molecules great versatility, and what effect do alternating double bonds have?

Carbon can self-associate into chains/rings and can form double bonds; alternating ("conjugated") double bonds make a molecule coloured, with more double bonds shifting colour towards red (e.g. beta carotene, haem, chlorophyll)

3
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Name five biologically important chemical groups and their structures.

Hydroxyl (-OH), carbonyl (-C=O), carboxyl (-COOH ↔ -COO-), amino (-NH2 ↔ -NH3+), sulfhydryl (-SH), and phosphoryl (-PO3)

4
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List three biologically important properties of organic molecules linked to their chemical groups.

1) Solubility in water; 2) ability to form weak, non-covalent bonds; 3) ability to bind metal ions

5
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Why are some organic molecules soluble in water, and what happens with very large molecules instead?

Polar groups (e.g. -OH) form hydrogen bonds with water, letting small molecules join the water network and dissolve; very large molecules may instead form a gel (e.g. cytoplasm, cartilage, vitreous humour)

6
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How do weak, non-covalent bonds help molecules, and how do organic molecules bind metal ions?

Ionic/hydrogen bonds can cross-link distant parts of a chain (giving a more resilient shape) or allow temporary binding between molecules; nitrogen atoms in ring structures form dative covalent bonds with metal ions (e.g. haem binds Fe2+, chlorophyll binds Mg2+)

7
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What is the general hierarchy of biopolymer assembly, and what are condensation and hydrolysis reactions?

Monomer → dimer → oligomer → polymer; condensation reactions join monomers and release water; hydrolysis reactions break polymer bonds by adding water, releasing free monomers

8
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Match each type of monomer to its resulting polymer.

Monosaccharides → polysaccharides; amino acids → polypeptides (proteins); mononucleotides → polynucleotides (DNA/RNA); fatty acids & glycerol → triglycerides (fats & oils)

9
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What is the general chemical formula of a carbohydrate, and what is another name for carbohydrates?

CH2O (a "carbon hydrate"); also called glycans (hence "glycobiology")

10
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How are monosaccharides classified by size and by chemical family, and what suffix do most sugar names share?

By size: triose, pentose, hexose; by chemical family: aldose (aldehyde group) or ketose (ketone group); most simple sugar names end in "-ose" (e.g. glucose, sucrose, lactose)

11
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What is glucose, chemically, and what is the difference between alpha and beta glucose?

An aldose hexose with molecular formula C6H12O6; alpha and beta glucose are structural isomers differing in the orientation of the -OH group at carbon 1

12
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What is a disaccharide, and describe Benedict's test for reducing sugars.

Two monosaccharides joined by a glycosidic bond (alpha or beta linkage), e.g. glucose+fructose or glucose+galactose; Benedict's test: mix sample with Benedict's solution and boil — sugars with an aldehyde group turn the solution from blue to a colour change (orange/red) as copper sulfate is reduced (disaccharides may need acid hydrolysis first)

13
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What is a polysaccharide, and how can the chains be arranged?

Many monosaccharides/disaccharides joined together, forming linear chains (e.g. amylose, cellulose) or branched chains (e.g. amylopectin, glycogen)

14
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List the three main functions of carbohydrates.

1) Energy source/storage (sugars, starch, glycogen); 2) structural support (cellulose, chitin, peptidoglycan); 3) molecular tags (oligosaccharide trees, e.g. blood group antigens)

15
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Compare starch and glycogen as energy storage polysaccharides.

Both are glucose polymers with identical chemical composition; starch (plants) is a mix of linear (amylose) and branched (amylopectin) forms, while glycogen (animals) is only the branched form

16
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Describe the glycosidic linkages in branched glucose polymers like glycogen/amylopectin, and describe the iodine test for starch.

Main chain = α(1→4) linkages, branches = α(1→6) linkages; iodine test: add iodine solution — starch/glycogen turns blue-black as iodine concentrates within the helical structure

17
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List the structural polysaccharides in plant cell walls, fungal cell walls/arthropod exoskeletons, and bacterial cell walls.

Plant cell walls: cellulose; fungal cell walls/arthropod exoskeletons: chitin; bacterial cell walls: peptidoglycan

18
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How does cellulose differ chemically from starch, and what is chitin made of?

Cellulose = glucose polymer with β(1→4) linkages (vs starch's α(1→4) linkages), making it structurally rigid; chitin = polymer of N-acetylglucosamine (NAG) with β(1→4) linkages

19
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What is a lipid (Greek origin and definition), and what is the difference between a fat and an oil?

From Greek "lipos" (fat); a broad category of hydrophobic molecules (fats, oils, waxes, cholesterol); fat = solid at room temperature, oil = liquid at room temperature

20
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List the main functions of lipids in the body.

Main energy store (triglycerides), structural support/cushioning, thermal/electrical insulation, forming membranes (phospholipids/cholesterol), waterproofing (waxes), and forming steroid hormones

21
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Describe the structure of a triglyceride and why it is an efficient energy store.

Three fatty acid chains attached to a glycerol backbone via condensation; very hydrophobic, making it compact and energy-dense

22
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Compare the energy storage of triglycerides versus glycogen.

Triglycerides store ~38 kJ (9 kcal)/g and remain ~100% lipid; glycogen stores ~17 kJ (4 kcal)/g and also carries ~2g of water per gram stored, making it far less energy-dense

23
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Describe the grease spot test and the emulsion test for lipids.

Grease spot test: spot sample on filter paper and dry — lipids leave a translucent mark; emulsion test: mix sample with ethanol, then add to water — lipids form a cloudy emulsion

24
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How does a phospholipid differ from a triglyceride, and why does this make it form a membrane bilayer?

A phospholipid has only two fatty acids, with a phosphate (or more complex) group in the third position instead of a fatty acid; this gives it a hydrophobic tail and hydrophilic head, so it spontaneously forms a bilayer in water

25
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What is a fatty acid structurally, and what are the three saturation categories?

A long-chain (12-24C) hydrocarbon carboxylic acid; saturated (no double bonds), monounsaturated (one double bond), polyunsaturated (more than one double bond)

26
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How does the number of double bonds affect a fatty acid's melting point, and what are essential fatty acids?

More (cis) double bonds cause kinking, increasing molecular motion and lowering melting point (more oil-like); essential fatty acids (omega-3 e.g. α-linolenic acid, omega-6 e.g. linoleic acid) cannot be made by the body and must come from the diet

27
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What roles do fatty acids play in membrane phospholipids?

Chain length affects bilayer thickness; degree of unsaturation affects membrane fluidity; composition is tissue-specific (e.g. brain is rich in omega-3/6); some fatty acids are precursors to signalling molecules

28
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What is a wax, structurally, and give a biological example of its use.

A fatty acid joined to a fatty alcohol, forming long hydrophobic, solid chains; used for waterproofing leaves/honeycombs and for buoyancy/sonar in sperm whales

29
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Describe the structure and membrane function of cholesterol.

Four fused rings, a hydrophobic tail, and a hydroxyl group; it fits between phospholipids and stiffens the membrane, protecting its integrity at both high and low temperatures

30
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List four steroid hormones derived from cholesterol.

Cortisol (stress hormone), aldosterone (kidney function), progesterone/oestrogen/testosterone (sex hormones), and vitamin D