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BIOC 2580 Final Exam Review Questions with Solved Solutions 2025 Updated.

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Commonly occurring saturated fatty acids - Answer 1. Laurate - 12 Carbons 2. Myristate - 14 Carbons 3. Palmitate - 16 Carbons 4. Stearate - 18 Carbons 5. Arachidate - 20 Carbons Features of commonly occurring fatty acids - Answer 1. Have an even number of carbon atoms 2. Unbranched 3. Double bonds commonly found in a cis configuration (introduces kinks) 4. PUFAs have methylene-bridged bonds (not conjugated) 5. Bond pattern = double-single-single-double Solubility and Melting Point of Fatty Acids - Answer Solubility decreases as the chain length increases Melting Point decreases as the chain length decreases decreases as the number of double bonds increases Derivatives of fatty acids - Answer 1. Alcohol + Carboxylic acid = Ester 2. Acid + Carboxylic acid = Acid Anhydride Triacylglycerols (triglycerides) - Answer A glycerol molecule esterified to three fatty acid molecules; the most common form of fat storage in the body Overall nonpolar and hydrophobic Reactions with phosphoric acid - Answer 1. Phosphoric acid + Alcohol = Phosphate ester 2. Phosphoric acid + Acid = Phosphoanhydride Phosphate derivatives - Answer - Phosphoric acid (H3PO4) is a triprotic acid - Represented by the notation Pi (inorganic phosphate)

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BIOC 2580 Final Exam Review
Questions with Solved Solutions 2025
Updated.
Commonly occurring saturated fatty acids - Answer 1. Laurate - 12 Carbons

2. Myristate - 14 Carbons

3. Palmitate - 16 Carbons

4. Stearate - 18 Carbons

5. Arachidate - 20 Carbons



Features of commonly occurring fatty acids - Answer 1. Have an even number of carbon atoms

2. Unbranched

3. Double bonds commonly found in a cis configuration (introduces kinks)

4. PUFAs have methylene-bridged bonds (not conjugated)

5. Bond pattern = double-single-single-double



Solubility and Melting Point of Fatty Acids - Answer Solubility

decreases as the chain length increases



Melting Point

decreases as the chain length decreases

decreases as the number of double bonds increases



Derivatives of fatty acids - Answer 1. Alcohol + Carboxylic acid = Ester

2. Acid + Carboxylic acid = Acid Anhydride



Triacylglycerols (triglycerides) - Answer A glycerol molecule esterified to three fatty acid
molecules; the most common form of fat storage in the body

Overall nonpolar and hydrophobic



Reactions with phosphoric acid - Answer 1. Phosphoric acid + Alcohol = Phosphate ester

,- Phosphorylation adds negative charges to molecules leading to an INCREASE in water solubility



Glycerophospholipids (phosphoglycerides) - Answer - Glycerol backbone bound by ester
linkages to two fatty acids and phosphodiester link to polar head

- Amphiphatic

- Form lipid bilayers



Amphiphatic - Answer A chemical or molecule that has a hydrophilic head and hydrophobic
tail used to transport fat



Lipids aggregate into structures in water - Answer - Fatty acids aggregate to form roughly
spherical micelles

- Hydrophobic tails of phospholipids are too bulky to pack together; aggregate into bilayers,
which spontaneously fold back on themselves to form liposomes or vesicles



Micelles are - Answer lipids surrounded by bile salts



Analysis of Lipids - Answer - homogenized in chloroform/methanol/water

- separated based on polarity on a column of silica gel or through TLC

- trans-esterification

- then gas-liquid chromatography or high-performance liquid chromatography is used to
separate the fatty acids



Adsorption chromatography - Answer a technique in which solute equilibrates between the
mobile phase and adsorption sites on the stationary phase



Thin Layer Chromatography (TLC) - Answer non-polar lipids move father than the polar lipids



Carbohydrates - Answer the starches and sugars present in foods



Chemical properties of monosaccharides - Answer - very water-soluble

- poorly soluble in inorganic solvents (ether or hexane)

- colourless

, 2. at least TWO carbons bearing hydroxyl (alcohol) groups



Trioses - Answer three carbon sugars



Fisher Projection - Answer - Horizontal lines = wedges/ out of the page

-Vertical lines = dashed/ into the page



Perspective Formula - Answer - Solid wedge shaped bonds project in-front

- Dashed bonds point away



Monosaccharides contain ______________________ - Answer chiral carbons, which give rise
to the occurrence of optically active isometric forms



Enatiomers - Answer - mirror images that differ at every chiral carbon atom

- commonly called "left-handed" and "right-handed" forms

- have IDENTICAL chemical properties

- DIFFER in optical activity



Diastereomers - Answer - monosaccharides with more than one chiral carbon with
stereoisomers that differ in handedness at some carbon atoms but not others

- do NOT have the same chemical properties



Sugars are named as ____ "right-handed" or L "left-handed" sugars, depending on how they are
drawn in a Fischer projection - Answer D, L



D and L sugars - Answer - A sugar is a "D" sugar if the chiral carbon atom furthest away from
the carbonyl group has the same configuration as D-glyceraldehyde



Epimers - Answer Pair of sugars that is identical except for the configuration at one carbon
atom



A sugar with n chiral centres has 2^n stereoisomers - Answer ex: An aldose with 5 carbons has
3 chiral centres

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