Paper 2

    Cards (324)

    • Alleles that are neither dominant nor recessive to one another, so both alleles are always expressed in the phenotype.
      Codominant
    • The inheritance of a single gene
      Monohybrid inheritance
    • Physical, behavioural, biochemical expression of an organisms genotype
      Phenotype
    • The type of genes an individual has

      Genotype
    • Alles that is always expressed in the phenotype
      Dominant
    • Only expressed in the phenotype when homozygous
      Recessive
    • Alleles that are neither dominant nor recessive to one another, so both alleles are always expressed in the phenotype.
      Codominant
    • both alleles are the same
      Homozygous
    • The inheritance of a single gene
      Monohybrid inheritance
    • Physical, behavioural, biochemical expression of an organisms genotype
      Phenotype
    • Both alleles for a specific gene are different
      Heterozygous
    • The type of genes an individual has
      Genotype
    • Position of a gene on a chromosome
      Loci
    • Alles that is always expressed in the phenotype
      Dominant
    • A set of instructions for a specific polypeptide

      Gene
    • Only expressed in the phenotype when homozygous
      Recessive
    • both alleles are the same
      Homozygous
    • Both alleles for a specific gene are different
      Heterozygous
    • Position of a gene on a chromosome
      Loci
    • A set of instructions for a specific polypeptide

      Gene
    • Phosphinate ions (H2PO2-) react with hydroxide ions to produce hydrogen gas as shown.
      H2PO2- + OH− →HPO32- + H2
      A student completed an experiment to determine the initial rate of this reaction.The student used a solution containing phosphinate ions and measured the volume of hydrogen gas collected every 20 seconds at a constant temperature.Figure 1 shows a graph of the student's results
      Use the graph in Figure 1 to determine the initial rate of reaction for this experiment.
      State its units. Show your working on the graph.
      above 5 cm3s-1
    • State the relationship between the initial concentration of phosphinate and time (t).
      Deduce the order of the reaction with respect to phosphinate.
      initial concentration of phosphine squared FISH 1/t
      2nd order
    • REVIEW GAS SYRINGE DIAGRAM
    • Deduce the overall effect on the rate of reaction when the concentrations of both
      L and M are halved.
      rate multiplied by 1/8
    • The rate of reaction is 0.0250 mol dm-3 s-1 when the concentration of L is 0.0155 mol dm-3
      Calculate the concentration of M if the rate constant is 21.3 mol-2 dm6 s-1
    • Define the term overall order of reaction.

      sum of the order with respect to each reactant in the rate equation
    • Draw a circle around any chiral centre(s) in Figure 3.
      2nd carbon from the left
    • Identify the functional group(s) in the prilocaine molecule

      amide & amine
    • Prilocaine is completely hydrolysed in the human body to give a mixture of products.
      Draw the structures of the two organic products formed in the complete hydrolysis of prilocaine in acidic conditions.
      benzene-NH3+
      COOHCH(CH3)NHCH2CH2CH3
    • Isomer F is the active compound in the medicine ibuprofen.In the manufacture of ibuprofen both isomers F and G are formed. An enzyme is then
      used to bind to isomer G and catalyse its hydrolysis.After the products of hydrolysis of G are removed, a pure sample of isomer F is
      collected.
      Explain how a structural feature of this enzyme enables it to catalyse the hydrolysis of
      isomer G but not the hydrolysis of isomer F.
      each enantiomer is stereospecific and so is complementary to the highly specific tertiary structure active site
    • Identify the isomer(s) that would react when warmed with acidified potassium dichromate(VI).
      State the expected observation when acidified potassium dichromate(VI) reacts.

      T,R,S,Q
      solution turns from orange to green
    • Identify the isomer(s) that would react with Tollens' reagent. State the expected observation when Tollens' reagent reacts.
      T
      silver mirror formed
    • Separate samples of each isomer are warmed with ethanoic acid and a few drops of concentrated sulfuric acid. In each case the mixture is then poured into a solution of sodium hydrogencarbonate.
      Identify the isomer(s) that would react with ethanoic acid.
      Suggest a simple way to detect if the ethanoic acid reacts with each isomer.
      Give a reason why the mixture is poured into sodium hydrogencarbonate solution.
      Q,R,S,P
      because an ester is formed between the alcohol and carboxylic acid a sweet smell is given off
      to neutralise any excess acid
    • State the type of structural isomerism shown by isomers P, Q, R and S.
      Position Isomerism
    • Describe fully how infrared spectra can be used to distinguish between isomers R, S and T.
      Use data from Table A in the Data Booklet in your answer.
      Isomer T will have a peak at 1680-1750cm-1 to show the presence of a C=O group.
      Both isomer R and T will have peaks at 3230-3550cm-1 to show presence of the O-H alcohol group. However, to distinguish between isomer R and T you need to look at the fingerprint region below 1500cm-1 an compare it to a database of known compounds
    • State why mass spectrometry using electrospray ionisation is not a suitable method to
      distinguish between the isomers.
      same Mr value, needs high resolution mass spectroscopy
    • Describe the instruction that is missing from step 4 of the method. Justify why this step is necessary.

      reweigh the weighing boat by itself to calculate an exact mass
    • Suggest a suitable piece of apparatus to measure out the ethanoic anhydride in
      step 5.
      pipette
    • Identify a hazard of using concentrated phosphoric acid in step 6.

      it may irritate skin as its corrosive
    • Complete the equation for the reaction of salicylic acid with ethanoic anhydride to
      produce aspirin.
      ethy ethanoate
      ethanoic acid