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CED
CED
*Po, Michaela P.
Coleen Casuga
Dona Macarans
Luigi Estorninos
ABSTRACT
The group is expected to determine the total amount of acidity of each of the sample used in this
experiment. In order to achieved this goal, the group prepared and standardized a basic titrant NaOH with
KHP solution aided with a phenolphthalein indicator. The experiment proper labeled the standardized NaOH
solution as its titrant to its analytes, the acid-containing samples. Necessary data were gathered during the
standardization up to the experiment proper to get the computed values that will be of great help to the
titratable acidity’s determination. It is to conform whether all of the sample will reach the same endpoint
during the procedure of this activity by calculating the total amount needed in each of the sample to obtained.
INTRODUCTION
Titration, process of chemical analysis in which the quantity of some constituent of a sample is
determined by adding to the measured sample an exactly known quantity of another substance with which
the desired constituent reacts in a definite, known proportion. The process is usually carried out by gradually
adding a standard solution (i.e., a solution of known concentration) of titrating reagent, or titrant, from
a burette, essentially a long, graduated measuring tube with a stopcock and a delivery tube at its lower end.
The addition is stopped when the equivalence point is reached.
At the equivalence point of a titration, an exactly equivalent amount of titrant has been added to the
sample. The experimental point at which the completion of the reaction is marked by some signal is called
the end point. This signal can be the colour change of an indicator or a change in some electrical property that
is measured during the titration. The difference between the end point and the equivalence point is the
titration error, which is kept as small as possible by the proper choice of an end-point signal and a method for
detecting it.
MATERIALS/REAGENTS
SAMPLES
Sample Juices (Powdered)
Calamansi
Honey dew
Dalandan
Vinegar (Variants)
Datu Puti
Silver Swan
Extract
Lemon
REAGENTS’ PREPARATION/PROCEDURE
Standard solution of 0.10 M NaOH
Needed reagent/s:
NaOH pellets
Others: Distilled water
Procedure:
1. The students weighted 4.0 grams of NaOH pellets in analytical balance
2. They dissolved it in 100 mL distilled water.
3. After dissolving it properly, transfered it into a clean and dry volumetric flask.
4. Dilute solution in a 1L beaker containing 900 mL of distilled water (total volume would be 1 L)
Phenolphthalein Indicator
Needed reagent/s:
Phenolphthalein
Ethanol
Procedure:
Needed reagent/s:
KHP
METHODOLOGY/PROCEDURE
In order to achieve the goal, the students pipetted 10 mL per powdered sample solutions and 3 mL per
vinegar and lemon extract and gently dispensed it into their respective Erlenmeyer Flasks, they diluted it with
100 mL distilled water and mixed, they added 3 drops of the phenolphthalein indicator in each Erlenmeyer
flasks containing the sample. They titrated using the standardized NaOH solution as the titrant and the acid-
containing samples as the analyte. The endpoint of the solution that had been titrated with the 0.10M NaOH
should be faint pink.
This table shows the different data needed to standardize the titrant of the experiment, NaOH, with the help
of KHP. The standardization was compared in 3 trials where each flask contained an ideal amount of 0.100
grams of KHP each. NaOH was then titrated to these trials and data were noted after each trials showed the
end point. The Molarity of NaOH was computed after getting various data values (such as KHP’s weight and
NaOH’s volume) with the formula given. The Molarity will show the results if the preparation of the titrant was
correctly calibrated to its goal molarity (in this case, it was 0.10 M) by comparing it to the goal value. The
closer its value is to the goal value, the better.
The Average column shows the computed mean of the Molarity of NaOH (column 4). This would aid the
computation of the %RSD, the one that measures the scattering of numbers in a particular data set around the
mean. By having a value of 5.30 % as the standardization’s %RSD, this indicated that there is a low percent of
scattering thus, the distance of the values of Molarity of NaOH to the mean were near each other.
In table 2, the group collected various data from other groups to calculate the average amount of NaOH
titrated in every sample given. This table also helped the group to compare the different set of data values
across other groups to see if the titrated amount of NaOH across different types of samples were near each
other for precision issues. The computed average would greatly affect and aid the computation for the most
important findings of this experiment, the sample’s individual acidity.
Table 4 showed the computed values that are necessary for the completion of the most important set of
values to be computed in this experiment, the values of samples concerning their Titratable Acidity. In each
acid-containing sample, the values that were used for titrated NaOH (named as NaOH used in the table) were
the average titrated NaOH from table 2 where the different data values were collected from different groups
to garner their respective average titrated titrant. The Molarity of the NaOH value used in the table was the
average Molarity indicated in table 1 (data were gathered through the titrant’s standardization). The volume
sample (in mL) and the correction factor used were given and indicated as instructed in the experiment
proper. All the said values were vital and greatly needed to compute for the titratable acidity of each sample.
The Titrated Acidity values of the samples can be viewed in the last column wherein in can be used for
comparison and other necessary uses it may be of aid. The final values of titratable acidity showed that
vinegar variants (Datu Puti and Silver Swan) have different percentage of acidity thus, breaking the
connotation that every vinegar’s just the same even in their compositions.
CONCLUSION
In this experiment, it was greatly revealed that there is a difference between the samples containing acetic
acid and those who contained citric acid (excluding their correction factor). Among the six samples given
(three of them are powdered and three are extracted/in their “pure” form before the instructed dilution),
those who received high titratable acidities were the samples containing their “pure”/extracted forms. This
means that there is a high concentration of acid components in the said samples. Those samples who were
processed to be in the powder form garnered a titratable acidity of less than 1%, a remarkably low value
compared to the samples that were unprocessed. This may mean that as their form is being reduced and is
processed, their acidity will also decline and it makes them less acidic compared to their original fruit
counterparts. Thus, with these results, the assumption concerning the difference of samples containing
different types of acids were proven.
APPENDIX
APPENDIX A: COMPUTATIONS
For “Table 1: Standardization of 0.10 M NaOH with the use of KHP’s” used formulas and computations:
Formula for the Molarity of NaOH (Standardization of 0.10 M of NaOH (standard solution)):
𝑤𝑡. 𝑜𝑓 𝐾𝐻𝑃
𝑀 𝑁𝑎𝑂𝐻 = 𝑀𝑀 𝐾𝐻𝑃 𝑥 1000
𝑚𝐿 𝑜𝑓 𝑁𝑎𝑂𝐻 𝑢𝑠𝑒𝑑
TRIAL 1:
0.100 g.
𝑀 𝑁𝑎𝑂𝐻 = 204.22 𝑥 1000
6 mL
𝑴 𝑵𝒂𝑶𝑯 = 𝟎. 𝟎𝟖𝟏𝟔 𝐌
TRIAL 2:
0.100 g.
𝑀 𝑁𝑎𝑂𝐻 = 204.22 𝑥 1000
6.6 mL
𝑴 𝑵𝒂𝑶𝑯 = 𝟎. 𝟎𝟕𝟒𝟐 𝐌
TRIAL 3:
0.100 g.
𝑀 𝑁𝑎𝑂𝐻 = 204.22 𝑥 1000
6.2 mL
𝑴 𝑵𝒂𝑶𝑯 = 𝟎. 𝟎𝟖𝟏𝟑 𝐌
Σ𝑥
𝐴𝑣𝑒𝑟𝑎𝑔𝑒 𝑚𝑜𝑙𝑎𝑟𝑖𝑡𝑦 =
𝑛
Whereas:
𝑆𝐷
% 𝑅𝑆𝐷 = 𝑥 100
𝑀𝑜𝑙𝑎𝑟𝑖𝑡𝑦 𝐴𝑣𝑒𝑟𝑎𝑔𝑒
Whereas:
0.004188476254
% 𝑅𝑆𝐷 = 𝑥 100
0.0790
% 𝑹𝑺𝑫 = 𝟓. 𝟑𝟎%
For “Table 2: Average Result of Titrated NaOH’s” used formula and computation:
Formula for the Titrated NaOH
Σ𝑥
𝐴𝑣𝑒𝑟𝑎𝑔𝑒 𝑡𝑖𝑡𝑟𝑎𝑡𝑒𝑑 𝑁𝑎𝑂𝐻 =
𝑛
Whereas:
LEMON EXTRACT
𝑨𝒗𝒆𝒓𝒂𝒈𝒆 𝒎𝒐𝒍𝒂𝒓𝒊𝒕𝒚 = 𝟕. 𝟎𝟖 𝐦𝐋
POWDERED HONEY LEMON JUICE
𝑨𝒗𝒆𝒓𝒂𝒈𝒆 𝒎𝒐𝒍𝒂𝒓𝒊𝒕𝒚 = 𝟕. 𝟑𝟕 𝐦𝐋
𝑨𝒗𝒆𝒓𝒂𝒈𝒆 𝒎𝒐𝒍𝒂𝒓𝒊𝒕𝒚 = 𝟓. 𝟗𝟕 𝐦𝐋
For “Table 4: Determination of Titratable Acidity (in % w/v)” used formulas and computations:
Where:
LEMON EXTRACT
Correction Factor:
Citric acid anhydrous: 0.064
Acetic Acid: 0.060