exam questions

Cards (12)

  • compare and contrast the structures of saturated and unsaturated fatty acids (4)
    • (They both have) hydrocarbon tails
    • (They both have) a (carboxylic) acid / -COOH group at one end
    • Saturated has more hydrogen/H atoms / only C-C single bonds
    • Unsaturated has C=C double bonds
    • Unsaturated can have kinked chains / saturated has straight chains
  • compare the structure of alpha and beta glucose
    -        Both hexose sugars / contain 6 carbon atoms
    -        Both have a ring structure
    -        Carbon 6 sticks out above/below the ring
     
    -        The location/orientation of the -H and -OH group on carbon 1
    -        Alpha glucose has the H above carbon 1 and the OH group below
    -        Beta glucose has the H below carbon 1 and the OH group above
  • state 2 features of glycosidic bonds that form between 2 monosaccharides in a condensation reaction
    -       A glycosidic bond is) formed from 2 -OH groups (on separate monosaccharides)
    -       Strong, covalent bond
    -       Act as a bridge via one oxygen atom / are formed -O- etc
    -       Links either C1 to C6 or C1 to C4
  • explain the name of the type of reaction that forms the carbohydrates in part a from their monomers (2)
    -       A condensation reaction where a water molecule is released from the reaction as a by-product.
  •  state 2 features of starch and explain how these features allow starch to act as a storage substance(4 marks)
    • Feature 1: Branched chains
    • Easy to remove glucose molecules/ fast breakdown/easily hydrolysed
    • Feature 2: Insoluble
    • no osmotic effect
    • Feature 3: Coiled/helical/spiral structure
    • Can fit many molecules into a small area/compact
    • Feature 4: Large molecule OR long chain
    • Contains many glucoses molecules
     
     
  • explain how the structure of glycogen allows it to be an energy store(3)
    • polymer of glucose
    • to provide glucose for respiration
    • branched(1,6 glycosidic bonds)/ many terminal ends for rapid hydrolysis
    • compact to allow large amount of glucose/energy to be stored in a small space
  • Describe the reaction that joins two α-glucose molecules to form a disaccharide(2)
    • condensation reaction
    • producing a H20 molecule
    • forming glycosidic bonds
  • give one structural difference between amylose and amylopectin(1)
    • amylose is unbranched( only 1,4 glycosidic bonds)
    • amylopectin is branched(1,4 and 1,6 glycosidic bonds)
  • Explain how the structures of amylopectin and glycogen make them suitable for storing energy(3)
    • branched thus can be rapidly hydrolysed(to release glucose)
    • compact so more energy/glucose can be stored
    • insoluble thus does not affect osmosis
    • molecules too large to diffuse across cell surface membrane
  • Compare and contrast the structure of a disaccharide with glycogen(4)
    • both contain carbon, hydrogen and oxygen
    • both contain glycosidic bonds
    • both contain glucose
    • glycogen contains 1,4 and 1,6 glycosidic bonds whereas disacchariodes only one type of glycosidic bond
    • glycogen only contains glucose whereas disaccharides can contain glucose and other monosaccharides
  • describe the structure of an unbranched polysaccharide
    • made up of many monosaccharide components
    • joined together by condensation reactions/glycosidic bonds
    • only 1,4 glycosidic bonds present, no 1,6 bonds
  • describe how the structure of glycogen is related to its function as a storage molecule(2)
    • branched molecule for more rapid hydrolysis
    • compact so more can be stored