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How does hydrogen bonding occur between water molecules? Include diagram.
Water molecule are polar (meaning charge is unevenly distributed), hence contain d+ hydrogen atoms and d- oxygen atoms. Between water molecules, there is a force of attraction between the d+ H and d- O, so a weak hydrogen bond forms.

Name the 6 properties of water that are important for life processes. Relate each one to living organisms.
Cohesion/ surface tension - supports small insects eg. pond skaters.
Adhesion - Capillary action: movement of H2O through blood vessels and xylem.
Latent heat of evaporation - Acts as a coolant eg. sweat
High specific heat capacity - Maintains constant temperatures in cellular environments.
Density of ice - Insulating layer above lake water so fish can survive in winter.
Universal solvent - Medium for chemical reactions and transport eg. blood.
Explain hydrolysis and condensation reactions and provide examples in ALL biological molecules
Condensation: joining of two monomers - releases water
Hydrolysis: breaking down of a polymer - requires water
Lipids - H on glycerol and OH on fatty acid react x3 to form 3 ester bonds and 3 H2O
Carbs - OH groups on C1 and C4 react to form a 1,4 glycosidic bond and H2O
Protein - OH group (in carboxyl group) and H (on amine group) react to form peptide bond and H2O
What are the chemical elements that make up each biological molecule?
Protein - C,H,O,N,S
Lipids - C,H,O
Carbs - C,H,O
Nucleic acid - C,H,O,N,P
Draw an alpha and beta glucose molecule. Describe the differences and similarities between them.
Similarities:
Hexose ring structure
Same molecular formula - C6H12O6
Same structure on C2,3,4,5 + 6
Difference:
Alpha - C1 has same position of OH and H as C4 (OH below)
Beta - C1 has opposite position of OH and H as C4 (OH above)

Draw a ribose molecule. Describe the difference between glucose and ribose.
Ribose only has 5 carbons - pentose molecule

Describe how the structure of starch (amylose/amylopectin) relates to its function.
Amylose: long chain of a-glucose molecules joined together by 1-4 glycosidic bonds to form an alpha helix (strengthened by H bonds
Function: Storage molecule in plants - compact, water insoluble
Amylopectin: Branched chain of a-glucose molecules with 1-4 bonds in chain and 1-6 bonds at branching points
Function: Storage molecule in plants - Compact, insoluble, branched so many free ends where glucose can be broken off for reactions (hydrolysis)

Describe how the structure of glycogen relates to its function.
Structure: Branched chain of a-glucose molecules with 1-4 bonds in chain and 1-6 bonds at branching points. Branches more frequently than amylopectin
Function: Storage molecule in animals and fungi - compact, many free ends to release glucose (hydrolysis)

Describe how the structure of cellulose relates to its function.
Structure: chains of b-glucose where every other molecule is rotated 180º. Many chains joined together by H bonds to form large sheet of cellulose
Function: Cell wall of plants - strong (many H bonds) and water insoluble.

Compare and contrast the structure of triglycerides to phospholipids.
Triglycerides: glycerol and 3 fatty acids joined by ester bonds, can be saturated or unsaturated (contains C=C), non-polar, stores energy.
Phospholipids: glycerol, 2 fatty acid and a phosphate group, hydrophilic head and hydrophobic tail, found in plasma membrane.

Explain the differences between saturated and unsaturated fatty acids
Saturated - all C-C, no C=C, higher melting point as they are more compact, so bonds harder to break
Unsaturated - contains C=C, lower melting point as they are less compact, so bonds easier to break
Describe the general structure of an amino acid.
Amine group - NH2
Central Carbon - CH
R group - a range of chemical groups different in each amino acids. 20 different amino acids naturally occuring in the human body.
Carboxyl group - COOH

Explain how a peptide bond forms.
Condensation reaction: bond forms between the C in carboxyl group and N in amine group, releasing H2O and forming peptide bond
Broken via hydrolysis reaction.

Outline the four different levels of protein structure.
Primary - the sequence of amino acids in a polypeptide chain. Determines all other levels of structure
Secondary - Polypeptide chain fold into a helix or b pleated sheet due to hydrogen bonding within the peptide chain.
Tertiary structure - 3D shape held in place by bond between the R groups in the polypeptide chains: covalent disulphide, ionic bonds, hydrophobic and hydrophilic interactions. Vital for function.
Quaternary - NOT ALL HAVE: Composed of 2+ polypeptide chains/subunits interacting and the interactions between peptide chains and prosthetic groups
Compare conjugated, globular and fibrous protein structures providing examples of each.
Conjugated - contains a prosthetic group ie. non-protein component. Example: Haemoglobin - contain Fe2+ in haem group
Globular proteins - compact, water soluble, spherical shape. Hydrophilic R groups on outside, hydrophobic inside. Example: Insulin - transported in bloodstream
Fibrous proteins - Long and insoluble. contain many hydrophobic R groups. Repetitive and organise structure with simpler 3D structure. Examples: Keratin, Elastin and Collagen - all have strength and flexibilty function so must be strong

Explain how to chemically test for reducing and non reducing sugars
Benedict’s test for reducing sugars:
Add equal parts Benedict’s solution to sample and warm in water bath (~80ºC)
Benedict’s test for non - reducing sugars:
Add 2cm of ~1.5M HCl and heat in water bath for 3 mins (to hydrolyse glycosidic bonds)
Cool and neutralise with NaHCO3, checking with pH paper
Carry out Benedict’s test as above
Results:
Red - Large, Orange - moderate, Green - traces, Blue - none
Explain how to chemically test for proteins, lipids and starch
Proteins - Biuret test for proteins
Add Biuret A and B. Lilac colour indicates protein present
Lipids - Emulsion test
Add ethanol, shake and add distilled water. Milky white emulsion indicates presence of lipid.
Starch - Iodine test
Add iodine solution. Blue black colour indicates presence of starch.