paper 1 practicals/ techniques Flashcards
(7 cards)
Suggest a method to measure the quantity of sugar in a solution
- carry out benedict’s test as above, then filter and dry precipitate
- find mass/weight
Describe a method to identify the concentration of glucose in an unknown solution.
- Make sugar solutions of known concentrations (e.g. dilution series)
- Heat a set volume of each sample with a set volume of Benedict’s solution for same time
- Use colorimeter to measure absorbance of light of each known concentration
- Plot calibration cruve - conc on x axis , absorbance on y
- Draw line of best fit. Repeat Benedict’s test with unknown sample and measure absorbance.
- Red off calibration cruve to find conc associated with unknown sample’s absorbance
Outline how chromatography could be used to identify the amino acids in a mixture
- Prepare the chromatography paper by drawing a pencil line near the bottom and placing small spots of the amino acid mixture and known amino acid standards along the line.
- Place paper in solvent (e.g., ethanol), ensuring the solvent level is below the spots. Leave it to develop in a covered container.
- As the solvent travels, different amino acids move at different rates depending on their solubility
- When the solvent has nearly reached the top, remove the paper and mark the solvent front. Dry the paper.
- Spray with a locating agent (e.g., ninhydrin) to make the amino acid spots visible.
- Compare the positions of the unknown spots with those of the known standards or calculate Rf values and match them to known Rf values.
Name 5 factors that affect the rate of enzyme-controlled reactions
- enzyme concentration
- substrate concentration
- concentration of inhibitors
- pH
- temperature
Common questions 1-4:
- Describe how temperature can be controlled.
- Describe how pH can be controlled.
- Why were the enzyme & substrate solutions left in the water bath for 10 mins before mixing?
- Describe a control experiment.
RP1: investigation into the effect of a named variable on rate of enzyme reactions
- Use a thermostatically controlled water bath + Monitor using a thermometer at regular intervals and
add hot / cold water if temperature fluctuates - Use a buffer solution+ Monitor using a pH meter at regular intervals
- So solutions equilibrate / reach the temperature of
the water bath - Use denatured enzymes (eg. by boiling)
- Everything else same as experiment, eg. same conc. /
volume of substrate (at start) and enzyme, same
type / volume of buffer solution, same temperature
common questions
- Suggest a safety risk and explain how to reduce this risk.
- Explain why using a colorimeter to measure colour change is better than comparison to colour standards.
- Explain a procedure that could be used to stop each reaction.
- Handling enzymes may cause an allergic reaction. Avoid contact with skin by wearing gloves and eye protection
- Not subjective + More accurate
- Boil / add strong acid / alkali -+ denature enzyme. Put in ice - lower kinetic energy so no E-S complexes form. Add high concentration of inhibitor -+ no E-S complexes form
state the formula for pH.
pH = −log10 ([H+])
H+ = hydrogen ion concentration of a solution