Experiments

  1. How many steps are there when Demonstrating Osmosis?
    • 10 steps
    • Soften busking tubing
    • Knot one end of each
    • Half fill with sucrose
    • Half fill with distilled water (control)
    • Eliminate air, knot the tops, wash and pat dry
    • Tie two ends
    • Observe turgidity and record mass
    • Hang from glass rod into beaker of distilled water
    • Remove, dry, and re-weigh, observe turgidity
    • Expected result
  2. What is the expected result when Demonstrating Osmosis?
    Expected result: the visking tubing that was immersed in a less concentrated solution swelled and tubing with distilled water stayed the same as the concentration gradient as the same.
  3. What equipment is involved when Demonstrating Osmosis?
    • Visking tubing
    • Funnel (to put solutions into tubing step 3+4)
    • Sucrose solution
    • Distilled water
    • Scale to weigh
    • Glass rod
    • Beaker (to hold distilled water)
  4. Why is visking tubing used when Demonstrating Osmosis?
    They’re semipermeable membranes that allow some molecules to pass.
  5. How many steps are there in examining a plant cell, stained and unstained using the light microscope ?
    • 12
    • Cut onion
    • Locate epidermis
    • Cut epidermis into small pieces
    • Place epidermis into water in petri dish
    • Drop of water on slide
    • Transfer epidermis into water
    • Apply cover slip (45*)
    • Lower cover slip
    • Dry gently and view the unstained
    • To stain, apply iodine and draw across using filter paper
    • Examine under microscope
    • Expected result: view of plant cell.
  6. When examining a plant cell, stained and unstained using the light microscope, what is the expected result?
    Expected result; view of plant cell.
  7. When examining a plant cell, stained and unstained using the light microscope, why is ye epidermis placed into water in a petri dish?
    To keep it turgid, prevents it getting plasmolysed.
  8. When examining a plant cell, stained and unstained using the light microscope, what equipment is used?
    • Knife (to cut onion in half)
    • Petri dish
    • Dropper (to place a drop of water on slide)
    • Paintbrush (to transfer the epidermis into the water)
    • Cover slip
    • Mounted needle (to lower cover slip at 45*)
    • Tissue (to dry gentle)
    • Microscope
    • Iodine to stain
    • Filter paper (to draw iodine across)
  9. When examining a plant cell, stained and unstained using the light microscope, what stain is used?
    Iodine (applied to one side and drawn across using filter paper)
  10. When examining an animal cell, stained and unstained, using the light microscope, how many steps are there?
    • 12
    • Swab inside cheek
    • Transfer sample to slide
    • Cover sample with water
    • Place cover slip at 45*
    • Lower cover slip with mounted needle
    • Dry slide
    • Examine under microscope
    • To stain- prepare like steps 1+2
    • Cover sample with methylene blue stain
    • Wash excess stain
    • Apply cover slip (as previously done)
    • Expected result- nucleus darker
  11. When examining an animal cell, stained and unstained, using the light microscope, what equipment is used? (9)
    • Inoculating loop (to swab)
    • Slide
    • Dropper (to drop water on sample)
    • Cover slip
    • Mounted needle (to lower cover slip)
    • Tissue (to dry if necessary)
    • Microscope
    • Methylene blue stain and dropper
    • Wash bottle (to wash excess stain from slide)
  12. When examining an animal cell, stained and unstained, using the light microscope, what is the expected result?
    Expected result: the nucleus stains darker than the cytoplasm as the DNA absorbed more stain.
  13. When examining an animal cell, stained and unstained, using the light microscope, why is the cover slip placed at the edge of the water at a 45* angle?
    To prevent trapping air bubbles which obstruct the view of the cells.
  14. When examining an animal cell, stained and unstained, using the light microscope, what is used to swab the inside of the cheek?
    Inoculating loop
  15. When conducting a qualitative test for fat, how many steps are there?
    • 6.
    • Cut up brown paper
    • Oil drops on paper A
    • Water drops on paper B (control)
    • Leave to dry
    • Hold up to light
    • Expected result- A translucent (positive)
  16. When conducting a qualitative test for fat, what equipment is needed?
    • Brown paper
    • Scissors (to cut brown paper)
    • Oil
    • Water (control)
    • Dropper
    • A light or window
  17. When conducting a qualitative test for fat, what is the expected result?
    Expected result: paper A positive- translucent spot and B negative- no translucent spot.
  18. When conducting a qualitative test for protein, how many steps are there?
    • 6.
    • Label 2 boiling tubes A and B
    • Place protein solution into tube A
    • Place water into tube B
    • Add Biuret reagent into each
    • Swirl tubes and observe colour
    • Expected result: A positive- lilac/violet, B negative- blue
  19. When conducting a qualitative test for protein, what is the expected result?
    Expected result: A positive - lilac/violet and B negative- blue
  20. When conducting a qualitative test for protein, what equipment is needed?
    • Boiling tubes
    • Protein solution
    • Water
    • Biuret reagent
    • Dropper
  21. What is used to test for protein?
    What is the control for this experiment?
    • Biuret reagent
    • Positive: lilac or violet
    • Negative: blue

    Control: water
Author
jacquelineglynn
ID
361899
Card Set
Experiments
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Questions
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