Biology RPs and Food Tests

0.0(0)
studied byStudied by 0 people
0.0(0)
full-widthCall Kai
learnLearn
examPractice Test
spaced repetitionSpaced Repetition
heart puzzleMatch
flashcardsFlashcards
GameKnowt Play
Card Sorting

1/12

encourage image

There's no tags or description

Looks like no tags are added yet.

Study Analytics
Name
Mastery
Learn
Test
Matching
Spaced

No study sessions yet.

13 Terms

1
New cards

What is the test for starch?

  • Add iodine solution to food.

  • Positive = blue-black

  • Negative = orange-brown

2
New cards

What is the test for glucose?

  • Add Benedict’s solution, then heat in water bath (~75°C).

  • Positive = green/yellow/orange/brick red (depends on amount)

  • Negative = stays blue

3
New cards

What is the test for lipids?

  • Add Sudan III stain and shake gently.

  • Positive = red layer forms on top

  • Negative = no separate red layer

🛑 Note: Sudan III is flammable and harmful — mention goggles and lab coat!

4
New cards

What is the test for proteins?

  • Add Biuret solution (sodium hydroxide + copper sulfate).

  • Positive = lilac/purple

  • Negative = blue

5
New cards

RP1 - Microscopy

Use a microscope to view cells (e.g., onion or cheek cells).

  • Prepare a slide (stain → cover slip → focus)

  • Use low → high magnification

  • Measure size using scale bar

6
New cards

RP2 - Culturing microorganisms

pre-inoculation:

  • sterilise Petri dish and agar

  • pass inoculating loop through flame

  • to kill unwanted bacteria

inoculation:

  • use swab to spread bacterium into agar

  • open the lid of dish as little as possible

  • to prevent microbes from the air entering

post-inoculation:

  • seal dish with tape

  • to prevent microbes from entering

  • incubate at 25°C

  • to allow growth of bacteria

7
New cards

RP3 - Osmosis in potatoes

  • Measure and record the mass of potato pieces

  • Place potato pieces into different concentrations of salt solution

    • Use at least 3 different concentrations of salt solution

  • Leave the potato pieces in the salt solutions for 30 mins

  • Remove potato pieces from salt solutions + blot dry

  • Calculate the change in mass (record new mass)

  • Repeat each concentration 2 more times

  • Calculate the mean change in mass

  • Plot percentage change

Control variables:

  • Use the same size + mass of potato pieces

  • Use same type of potato

  • Keep potato pieces in solution for same amount of time

  • Volume is solution

8
New cards

RP5 - Enzymes (amylase and pH)

Investigate how pH affects amylase breaking down starch.

  • Mix amylase + starch solution together with a buffer solution

  • At regular intervals,

  • Use iodine in spotting tile

  • Time how long until no starch remains (iodine stays orange)

  • Vary pH buffer

  • Control: temp, volume, concentration

Amylase and starch solutions are mixed together with a buffer solution to control the pH. The mixture is kept at 37°C using a water bath.

At regular intervals, drops of the mixture are added to iodine solution on a spotting tile. Iodine turns blue-black if starch is present.

The time taken for the iodine to stop turning blue-black is recorded. This shows how quickly starch has been broken down. The experiment is repeated at different pH values. The fastest reaction shows the optimum pH for amylase.

9
New cards

RP6 - Photosynthesis (light intensity + pondweed)

Measure rate of photosynthesis by counting bubbles/volume of oxygen.

  • A piece of pondweed is placed in water with sodium hydrogencarbonate to provide carbon dioxide.

  • Change light intensity by moving lamp

  • Count the number of oxygen bubbles released in a fixed time

  • (The closer the lamp the higher the LI)

  • Control: CO₂, temp, same pondweed

  • Use ruler for distance, stopwatch for timing

  • Optional: Use gas syringe for accuracy

As light intensity increases, the rate of photosynthesis increases until it reaches a maximum where another factor becomes limiting.

10
New cards

RP7 - plan and carry out an investigation into the effect of a factor on human reaction time

Reaction time is measured using a ruler drop test.

  • A ruler is held vertically and dropped without warning. The distance fallen before being caught is recorded and converted into reaction time.

  • Repeated several times

  • Calculate a mean

  • The investigation can be repeated while changing a factor such as caffeine intake, tiredness, distractions, or dominant vs non-dominant hand.

  • Using repeats improves reliability and helps identify anomalies.

11
New cards

RP8 - Investigate the effect of light or gravity on the growth of newly germinated seedlings.

Seeds are germinated and placed in a box.

For light experiments, light is allowed from one direction only. For gravity experiments, the box is rotated.

  • After several days, the direction of shoot and root growth is observed.

  • Shoots grow towards light (positive phototropism) and against gravity (negative gravitropism).

  • Roots grow downwards due to gravity.

  • This happens because auxin redistributes in the plant, causing uneven growth.

12
New cards

RP9 - Measure the population size of a common species in a habitat.

Use sampling techniques to investigate the effect of a factor on the distribution of this species.

  • Use a quadrat of 1m by 1m

  • Place the quadrats randomly

  • Using a random number generator to find the coordinates of 10 quadrats

  • Count the number of plants in each

  • Calculate the mean per quadrat

  • Find the area of the field

  • Find the population by multiplying the mean x area of field

13
New cards

RP10 - Investigate the effect of temperature on the rate of decay of fresh milk by measuring pH change.

Milk samples are placed at different temperatures.

  • The pH of each sample is measured at regular intervals using a pH probe or indicator.

  • As bacteria grow, they produce acids which lower the pH.

  • A faster decrease in pH shows a higher rate of decay.

  • Higher temperatures increase enzyme activity in bacteria, causing milk to spoil faster.