Preview

What Is Sodium Hypochlorite (Naocl) In Acetic Acid

Better Essays
Open Document
Open Document
854 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
What Is Sodium Hypochlorite (Naocl) In Acetic Acid
PurposeIn this experiment, sodium hypochlorite (NaOCl) in acetic acid mixture was used to oxidize emdo-borneol (an alcohol) to camphor (a ketone). The product would then be purified by sublimation and then be analyzed by Infrared spectroscopy and melting point test.

Procedure and ObservationsPlease refer to the lab manual and the carbon copy attached.

Data and CalculationsWeight of endo-borneol = 0.2013gNo of moles of endo-borneol = 0.2013g/154.25g mol-1 = 1. 305mmolSince one mole of endo-borneol should give one mole of camphorTheoretical yield of camphor = (1.305 mmol )( 152.23g mol-1) = 0. 1987gTheoretical melting point of camphor = 179.75 oCActual Yield of the product (camphor) = 9. 5360 - 9. 4873 = 0. 0487 g% Yield of the product = (100)*
…show more content…
In acidic solution, iodide ions should be oxidized by the hypochlorite ions to iodine and therefore gave a purple black color.

The result of this experiment was not very satisfactory, although the reaction was carefully controlled so that the temperature was kept more or less at 40oC. First of all, the yield of the product (24.5%) was quite low. This was mainly because of the fact that there was significant loss of materials during transfer of crystals and because of incomplete conversion of endo-borneol to camphor. It was observed that during swirling of endo-borneol to help it dissolve in acetic acid, some of them got stuck on the wall of the flask, and therefore was not being oxidized by the hypochlorite.

For improvement, it might be a good idea not to add all the acetic acid at one time, but left a little bit of it to wash down the endo-borneol stuck at the wall. The loss of crystals during transfer could be minimized by more careful handling. However, some loss seemed to be inevitable as it was impossible to get all the tiny crystals out from one flask to

You May Also Find These Documents Helpful

  • Better Essays

    Redox Area Lab Report

    • 741 Words
    • 3 Pages

    Iodine and Alcohol: No visible pieces of Iodine present in solution. Change of color from clear to dark brown.…

    • 741 Words
    • 3 Pages
    Better Essays
  • Better Essays

    Abstract: Using hypochlorous acid to convert secondary alcohol called cyclododecanol to the corresponding ketone which is cyclododecanone by oxidation.…

    • 708 Words
    • 3 Pages
    Better Essays
  • Satisfactory Essays

    What does the color change in #3 indicate? Water and IKI was in jar and the iodine caused the color change of the water.…

    • 354 Words
    • 2 Pages
    Satisfactory Essays
  • Powerful Essays

    commercial bleach lab

    • 501 Words
    • 3 Pages

    8) Titrate the solution with the 0.10 M sodium thiosulfate solution until the iodine color fades to a light color.…

    • 501 Words
    • 3 Pages
    Powerful Essays
  • Better Essays

    Isoborneol With Bleach

    • 1188 Words
    • 5 Pages

    Purpose: In this experiment, Green chemical procedures were applied to oxidize isoborneol to camphor using bleach (NaOCl), rather than the tradition chromium-based oxidizing reagents. The camphor was then purified using the process of sublimation.…

    • 1188 Words
    • 5 Pages
    Better Essays
  • Satisfactory Essays

    Ochem Lab

    • 394 Words
    • 2 Pages

    In this experiment, the secondary alcohol is selected over the primary alcohol. In many cases the primary alcohol can be oxidized all the way to a carboxylic acid. In order to achieve selectivity, sodium hypochlorite is used. It is reacted with acetic acid to form HOCl.…

    • 394 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    The Aldehyde Enigma

    • 817 Words
    • 4 Pages

    In the Cannizaro reaction an aldehyde is simultaneously reduced into its primary alcohol form and also oxidized into it 's carboxylic acid form. The purpose of this experiment is to isolate, purify and identify compounds 1 and 2 which contain 4-chlorobenzaldehyde, methanol, and aqueous potassium hydroxide. Compounds 1 and 2 are purified by crystallization. . The purified product will be characterized by IR spectroscopy and melting point.…

    • 817 Words
    • 4 Pages
    Good Essays
  • Powerful Essays

    W - Kinetics of the Reaction of a Food Colourant with Sodium Hypochlorite ..................... 31…

    • 7286 Words
    • 43 Pages
    Powerful Essays
  • Better Essays

    Development of an Equation

    • 1476 Words
    • 6 Pages

    Iodide reaction with hydrogen peroxide observations- The precipitate at the bottom turned into a red solid and the liquid solution was a dirty yellow color.…

    • 1476 Words
    • 6 Pages
    Better Essays
  • Good Essays

    A Grignard reagent was produced by reacting ~0.15 g of magnesium metal, stir vane, 0.80 mL of bromobenzene (0.70 mL) and anhydrous diethyl ether (20.0 mL) mixture in a 20-mL round-bottom flask (reflux apparatus). The apparatus was elevated from the hot plate and heated at 60°C for 15 minutes. Brownish-gray solution was observed. The remainder bromobenzene/ether mixture was added to the round bottom flask drop-wise with additional washing of ~2.0 mL of diethyl ether. Iodine (catalyst) was added to facilitate the reaction. Phenylmagnesium bromide was obtained upon cooling of the solution to room temperature. Benzophenone (1.09 g) and diethyl ether (2.0 mL) mixture was then reacted with the Grignard product for 15 minutes. Red solidified adduct was observed. Next HCl (6.0 mL) was added drop-wise to the adduct; bilayer of triphenylmethanol and inorganic impurities was observed. The mixture was then filtered using the reparatory funnel. The round-bottom flask was washed with additional ether (5.0 mL) and re-extracted. Sodium sulfate was then added to dry the solution. Aqueous solution was then decanted into an Erlenmeyer flask and evaporated in a hot water bath (50°C) with air until oily solid was observed. Hot petroleum ether (3.0 mL) was added drop-wise to dissolve the by-products and cooled to room temperature. Upon cooling, the crude was then vacuum filtered and collected. Hot Isopropyl alcohol was then…

    • 909 Words
    • 4 Pages
    Good Essays
  • Better Essays

    To start this experiment, 0.200g of (E) Stilbene, white salt like compound with no specific aroma, were added to a round bottom flask weighting 17.73g. Then 4mL of cold acetic acid, clear liquid with vinegar smell, were also added to the flask and the mixture with a flea stir bar was placed in sand bath for around 12 minutes until the (E) Stilbene was completely dissolved. Pyridinium tribromide (0.394g), a bright red powder, was added to the mixture, resulting in a fast change in the coloration of the first mixture from clear to an orange/brown liquid. The new reaction was placed back to the sand bath and the dark orange color, which was expected to fade, changed colors from first a light yellow to a cloudish yellow color with a bright yellow layer on top. This reaction occurred in a period of 7.5 minutes at constant stirring. After the time indicated by instruction was completed, 4mL of cold DI water were added in order to increase the polarity and agitate the precipitate without dissolving the sample. After this addition the mixture turned completely white with notorious solid at the bottom. This solid formed in the flask was collected through vacuum filtration with a Hirsch…

    • 1023 Words
    • 5 Pages
    Better Essays
  • Good Essays

    Experimental: Sodium metal was patted dry to remove any oil and was cat into small pieces. A dry 100cm3 round bottom flask was placed on a cork ring, on a balance and tarred sodium metal (0.6g) was placed into the flask. The flask was then attached to the dry reflux condenser and industrial methylated spirits (IMS, 15cm3) was added. Once all of the sodium has dissolved the solution was cooled to room temperature and the para-acetamidophenol (3.5g) was added. Ethyl iodine (3.0cm3) was slowly introduced to the mixture through the top of the condenser and the resulting in the mixture was boiled at reflux temperature for 20 minutes and was placed in a rotary evaporator to remove any excess solvent. Distilled water (40cm3) was added to the mixture and the flask was placed in ice until crystals were formed. The crude product was filtered using vacuum filtration the filtrates were washed with very little cold water and were left dry as much as possible.…

    • 652 Words
    • 3 Pages
    Good Essays
  • Good Essays

    The objective of this experiment was to learn the process of recrystallization and how this process removes the impurities from a pure solid compound. The methods used to achieve this objective were also hot vacuum filtration in order to remove suspended solid impurities, and isolating the pure acetanilide. In the next lab, percent recovered was obtained through weighing the acetanilide sample as well as comparing its melting point range.…

    • 464 Words
    • 2 Pages
    Good Essays
  • Better Essays

    Analysis of Bleach

    • 898 Words
    • 4 Pages

    1. Acidified iodide ion is added to hypochlorite ion solution and the iodide is oxidized to iodine.…

    • 898 Words
    • 4 Pages
    Better Essays
  • Good Essays

    Figure 4.2 and Figure 4.3 show the chromatogram for sample of Hurix’s Massage Balm and Serai Balm, respectively. Camphor and menthol have been detected in both samples. The peak of camphor compound is at retention time of 14.104 min for Hurix’s Massage Balm sample and Serai Balm sample is at 14.129 min. Meanwhile, the peak of menthol compound for Hurix’s Massage Balm sample is at 14.485 min and 14.405 min for Serai Balm…

    • 896 Words
    • 4 Pages
    Good Essays