I've got quite a lot of questions here sorry!
1. The pH of 0.10 M CH3COOH(aq) can be determined using its Ka value and, from the simplified equilibrium law, Ka= [H3O+]2/0.10. State two assumptions made in establishing this simplified relationship and explain why the [H2O] is not included.
- ?
2. A catalyst increases the proportion of‘‘successful’’ collisions by lowering the activation energy, but how does it lower the activation energy?
- is it just providing an alternative reaction pathway? (doesn't sound like it's enough)
3. CH3CH2OH is oxidised to CH3COOH by acidified Cr2O72-(aq).Write balanced half-equations for both the oxidation and the reduction?
- With the oxidation reaction CH3CH2OH + H2O(l) --> CH3COOH + 4H+(aq) + 4e-; are the states for ethanol and ethanoic acid both aqueous?
- And what is the reduction reaction?
4. The production of large biomolecules such as lipids, carbohydrates, proteins and DNA involve condensation reactions, i.e. water is a product. Describe the functional group changes that occur when lipids, carbohydrates and proteins are formed.
- carbohydrates: OH + OH -> ether/glycosidic links
- proteins: COOH + NH2 -> amide/peptide links
- lipids though?
5. Enzyme activity depends on the proteins tertiary structure. Changes in pH can disrupt this tertiary structure and denature the protein. Using aspartic acid as an example, explain how a change in pH can alter the charge on a side group in a protein chain.
- is it in low pH, the NH2 becomes NH3+
- in high pH the COOH becomes COO-
- are those sufficient?
6. Aspirin can be produced from reaction between salicylic acid and ethanoic acid. However the yield is significantly better if ethanoic anhydride is used and H2O is not a product. The theoretical yield is determined stoichiometrically from the amounts of reactants used. The actual yield is lower than the theoretical yield since the reaction reaches equilibrium. Explain, in terms of concentration changes and rates, how a reacting mixture of salicylic acid and ethanoic anhydride ‘‘reaches equilibrium’’.
- yeah im not sure here..
Ahh, any help at all in any of these would be greatly appreciated!
1. Water is the solvent and is the dominating species here; its concentration doesn't appreciably change at all and remains constant at around 55 M
An assumption is that the concentration of ethanoic acid stays constant; the actual equilibrium law would be [H3O+][CH3COO-]/([CH3COOH]-[CH3COO-]) to account for the change in concentration of the ethanoic acid.
2. It forms bonds to the reactants to lower the activation energy. Alternative reaction pathway? Not specific enough, although VCE chemistry doesn't really say so
3. Yes, states for ethanol and ethanoic acid are aqueous as they dissolve well in water.
Reduction of dichromate? Cr2O7 2- + 14H+ + 6e- => 7H2O + 2Cr 3+ I think
4. Lipids have esters?
5. Not quite; if you change the charges, then you form new ionic bonds/remove old ionic bonds depending on what charge change there is. For instance, if you go from R-NH3+ to R-NH2, you remove potential bonds between the NH3+ and a R-COO- group, for instance. Thus, the bonding in the tertiary structure is affected.
6. At equilibrium, the forwards and backwards reaction rates become equal and concentrations no longer change. Initially, the salicylic acid and the ethanoic anhydride are the only species present, so there is no back reaction. However, as the reaction progresses, more acetylsalicylic acid is formed, which increases the backwards reaction rate until the forwards and backwards rates are equal.