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Reflection

In this lab report, the student summarized their learning from 6 different labs covering topics like titration techniques, using a spectrophotometer, lipid extraction, microbiology techniques, and paper chromatography. Some key lessons included carefully delivering solutions, ensuring sterility in microbiology, and following steps properly like marking solvent levels in chromatography. The student realized the importance of precision and avoiding mistakes in experiments.

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0% found this document useful (0 votes)
3K views3 pages

Reflection

In this lab report, the student summarized their learning from 6 different labs covering topics like titration techniques, using a spectrophotometer, lipid extraction, microbiology techniques, and paper chromatography. Some key lessons included carefully delivering solutions, ensuring sterility in microbiology, and following steps properly like marking solvent levels in chromatography. The student realized the importance of precision and avoiding mistakes in experiments.

Uploaded by

api-383698554
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as DOCX, PDF, TXT or read online on Scribd
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REFLECTION

Lab 2

In this lab, we were doing titration techniques. For this lab, there are many precautions

should be taken. In this lab, I had make a mistake which is overshooting the endpoint of the

analyte. I realized that with a little mistake, it will cause error to our result. So most

importantly, take care not to overshoot the endpoint as the presence of large excess of titrant

will cause the resulting error. There are many others precautions that we should take. For

example, we must make sure that we used very clean glassware to avoid other substance mix

with our analyte or titrant. To deliver an accurate volume of solution, we must use pipette

rather than measuring cylinder. Besides, it is best to titrate into Erlenmeyer flask because we

can swirl it easily without danger of sloshing out the content. When doing this experiment, I

realized that we should work carefully and meticulously.

Lab 3

In this lab, we were using a spectrophotometer to measure the protein absorbance. For

this lab, there are many important things that we should know and apply. Firstly, we need to

measure the volume of all solution ( gelatin, H2O, biuret ) accurately. I did not transfered the

solution slowly into the cuvette, so the spectrophotometer cannot read the absorbance

accurately. So, we had to repeat the step again. The most important when doing this

experiment is to set the absorbance to zero and it will serve as a blank solution. Why ?

because we want to measure how much light is absorbed by protein alone. From this

experiment, I got to learn something new which is how to use the spectrophotometer properly

and learn about it uses.


Lab 4

In this lab, we need to extract and detect the presence of lipid in various sample of

foods. There are also some precaution that we should noted in this experiment. First of all, we

want to get the lipids to dissolve in the petroleum ether. We must make sure that the lipid is

dissolve completely. After that, we decant the petroleum ether to get the solid portion and

liquid portion. Next, we need to evaporate the petroleum ether. For this step, we must use hot

plate or allow the beaker to dry overnight but it will consume much time, so using a hot plate

or water bath is more efficient. Most importantly, we were reminded to not attempt to

evaporate the petroleum ether with a flame. As we know, ether is teribbly dangerous because

it is flammable and explosion hazard. From this experiment, I realized the importance and the

effects of content of lipid in our diet.

Lab 5

When doing a microbiological laboratory, there are many aspects that we need to pay

attentions. For example, in this lab, we need to produce isolated colonies on agar plate using

streak plate method and determined the effect of handwashing using various step. . For this

part, it is crucial to maintain a sterile work area surrounding us to make sure that the bacteria

do not affect our health and the people surrounding us. Unfortunately, when doing the streak

plate method, I forgot to sterile the loop with 70% ethanol. Next, we are required to do gram

staining to differentiate between the 2 major categories of bacteria which is gram positive and

gram negative. For this part, there is no problem as we had followed the step properly without

leaving even one step behind.


Lab 6

In this lab, we were used paper chromatography to separate plant pigments from a

plant using a hydrophobic solvent and is called chromatography techniques. In this lab, I had

to repeat the step over and over again because the leaf extract got dissolve in the solvent.

There are many step that we should follow properly. Firstly, the paper must be placed

vertically and straight into the test tube to prevent our mobile phase get bent. Moreover, we

must ensure that the leaf extract is above the solvent all the times. If it submerged in the

solvent, the extract would dissolve into the solvent and prevent them to separate. Most

importantly, we need to mark the solvent level when we removed it so the point at which the

solvent stopped could be noted in case the solvent kept advancing.

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