Larkin Lab Report- Titration

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    Cristian Rodriguez

    May 13, 2013

    Period 4

    Whos the One to Blame?

    Introduction:

    A titration is a lab technique used to determine the exact concentration of an

    unknown acid or base. Often times, acids and bases are identified based on their physical

    properties. An acid is a typically sour substance that gives away their hydrogen ions

    when dissolved in water with a base and turns litmus paper red. The characteristics of a

    base are the opposite of an acid. They absorb hydrogen ions and turn litmus paper blue

    The purpose of this lab is to identify who killed Mr. M by analyzing and matching the

    Molarity of the Crime Scene HCl acid sample to the Molarity of the suspects found in the

    investigation. In this lab, the acid samples will behave as the solvents of the solution or

    the substance that takes up most of the volume and the bases will behave as solutes or

    substances that take up less volume when both are blended. The result of this mixture

    should be a neutralization reaction, a reaction in which an acid and a base in an aqueous

    solution react to produce neutral water and salt. In addition, after the experiment, it will

    be necessary to identify the Molarity of HCl by using the formula (moles/ liters) in order

    to compare the different Molarity to find the killer.

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    Procedures:

    1. Before starting, the students wore their goggles on and obtained the following

    materials:

    A 50 ml graduated cylinder

    A 50 ml burette, stand, and cylinder

    A 125ml Erlenmeyer flask Phenolphthalein indicator

    Glass funnel

    2. The stopcock was turned towards the bottom and remained perpendicular to

    the tube of the burette in a closed position.3. The burette was filled with 1.0 M NaOH base. Then the initial volume was

    recorded.

    4. The graduated cylinder was utilized to measure 20ml exactly for each acid

    sample.5. 3 drops of phenolphthalein indicator were added to the acid samples ( the acid

    remained clear).6. The stopcock was opened until there was a slow stream of NaOH in order to

    titrate the unknown acid.

    7. When the drops fell, the flask was swirled and the coloring disappeared.

    Observations were recorded in the results section.8. When a solution was approaching neutralization, it became piker more rapidly

    and will later clear itself.

    9. Then, the stopcock was gently, partially opened and little drops were pouredinto the acid sample.

    10. When the coloring did not disappeared, the stopcock was quickly closed. If

    the solution had a very faint pink color, then it was a good titration. Though, if

    the titration was dark pink, it was necessary to redo the proceadures over intrial 2.

    11. The Final Volume of NaOH in the burette was recorded.

    12. The Total Volume (in mL) of NaOH was calculated. It neutralized thesuspects sample and the data was recorded.

    13. The burette was refilled with NaOH and the procedures were repeated with

    the other 3 samples.

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    Data:

    (Table 1): Data for in search of the Final Volume of NaOH

    Exact

    Volume of

    HCl (mL)

    Initial

    Volume of

    NaOH(mL)

    Final

    Volume of

    NaOH(mL)

    Total

    Volume of

    NaOHUsed in

    titration(mL)

    Molarity

    of HCl

    (M)

    Observatio

    / Notes

    Suspect A

    Kirkpatrick

    HCl Acid

    Trial

    1

    20mL 10mL 20mL 10mL .5M. -dark pink

    Trial

    2

    20mL 20.5mL 30mL 9.5mL -light pink

    Suspect B

    Larkin

    HCl

    Acid

    Trial

    1

    20mL 3mL 8.5mL 5.5mL -dark pink

    Trial

    2

    20mL 8.5mL 13mL 4.5mL .225M -light pink

    Suspect C

    Nguyen

    HCl Acid

    Trial

    1

    20mL 13mL 27mL 14mL .7M -light pink

    Trial

    2

    20mL 27mL 43mL 14mL -light pink

    Crime Scene

    HCl Acid

    Trial

    1

    20mL 1mL 5.5mL 4.5mL -dark pink

    Trial

    2

    20mL 5.5mL 9.5mL 4mL .2M -light pink

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    Calculation Table 2:

    Acid Sample 1. Moles of NaOH 2. Moles of HCl 3. Molarity of HCl

    (moles HCl/Liters HCl

    used)

    Suspect AMrs.Kirkpatrick

    .01 mol 0.1 mol HCl0.5 mol HCl

    Suspect B

    Mr. Larkin

    .0045 mol .0045 mol HCl

    0.23 mol HCl

    Suspect C

    Ms.Nguyen

    .014 mol .014 mol HCl 0.7 mol HCl

    Crime Scene

    Sample

    .004 mol .004 mol HCl 0.2 mol HCl

    Conclusion:

    At the end of the titration lab, it was concluded that Mr. Larkin is responsible for

    Mr. Mehkatarians death. The acid samples, the solvents of the solution, were mixed with

    drops of phenolphthalein and NaOH, both solutes, created a homogenous reaction. For

    example, the acid sample for Mrs. Kirkpatrick was mixed with both the phenolphthalein

    indicator and with NaOH, and turned the acid sample into a dark pink for the first trial

    and a light pink for the second trial. This indicates when the solution is light pink, it is a

    weak, less concentrates acid. However, if the acid was dark pink after the solvents were

    poured into it, then acid was strong thus more concentrated. After the experiment, the

    Moles HCl were found. But first, the equation was balanced forNaOH + HCL and

    obtained NaCl + H2O. The balanced equation demonstrates that an acid donates its

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    Hydrogen ions to the base when both are dissolved in water. When the moles of HCl

    were found and its Molarity, the Molarity of each acid sample, including the crime scene

    were compared in order determine the rue killer. In the end, the concentration of the acid

    sample of Mr. Larkin was similar to the sample found in the crime scene, indicating that

    Mr. Larkin was found guilty.

    Although the results and data were obtained, there were sources of error present

    as well. One source of error that affected the data was the testing materials such as the

    Erlenmeyer flask. The materials were not fully cleaned and perhaps the actual amount of

    NaOH needed when added to the HCl is inaccurate. As a result, multiple trials were

    performed for each acid sample, making trial 1 for each acid sample unreliable. Another

    source of error was the stand because it was loose. When NaOH was poured into the acid

    sample, the students had to read the scale of the 50mL burette; however, the burette was

    difficult to read because it was slanted. As a result, the column for the Final Volume of

    NaOH is unreliable. If the materials were fully rinsed before the experiment and if the

    stand was not slanting, the data could have been more accurate.

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