Preview

Reactions of butanols with hydrbromic acid

Good Essays
Open Document
Open Document
512 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Reactions of butanols with hydrbromic acid
Timothy Tran
T1058351
09/09/2014

Experiment 28: The reaction of Butanols with Hydrobromic Acid

Pre-lab

Objective:

The objective of this experiment is to synthesize 1-bromobutane and 2-bromobutane with different catalyst:substrate ratios to determine which ratio is the most economically favorable.

Discussion:

In this experiment, 1-butanol or 2-butanol will be converted to the corresponding alkyl bromide with HBR, while using sulfuric acid as a catalyst. The sulfuric acid will accelerate the chemical reaction with being consumed in the process, it will increase the concentration of the protonated alcohol, which then can form an alkyl bromide by either an SN1 or SN2 reaction.

The reaction for both mechanisms depends on the concentration of protonated alcohol and the catalyst should increase the rate of the reaction. This could increase the amount of alkyl bromide produced, but it could increase the side reactions as well which would reduce product yield. Therefore this experiment will test different ratios to determine the best cost ratio.

Procedure:

Reaction:
1. Assemble an apparatus for heating under reflux using a 50-mL round-bottomed flask, a water cooled reflux condenser, and a gas trap containing 1 M NaOH. The gas trap can be omitted if you under a fume hood.
2. Weigh 72.0 mmol of your assigned alcohol (1-butanol or 2-butanol) into the round-bottomed flask.
3. Cool the flask in ice water and under the hood cautiously add 10.0 mL (89 mmol) of 48% aqueous hydrobromic acid. Then add your assigned volume of concentrated sulfuric acid.
4. Drop in some boiling chips and heat the mix under reflux for one hour from the time the solution starts to boil.
Separation:
5. Codistill the alkyl bromide with the water present in the reaction mix, using a simple distillation apparatus (no additional funnel) with a graduated cylinder as the receiver.\
6. Stop the distillation when the distillate is no longer cloudy and the organic layer no

You May Also Find These Documents Helpful

  • Satisfactory Essays

    3. Weigh about 0.2 grams (+0.01 g) of the ground up tablet powder and transfer it to a clean 250 mL Erlenmeyer flask.…

    • 255 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Abstract: The objective of this experiment is to successfully perform a dehydration of a 2-butanol and a dehydrohalogenation of 2-bromobutane to form the products 1-butene, trans-2-butene, and cis-2-butene. It was found that a dehydration of 2-butanol yielded 4.6% 1-butene, 67.3% trans-2-butene, and 28.1% cis-2-butene, and a dehydrohalogenation of 2-bromobutane yielded 19.1% 1-butene, 69.9% trans-2-butene, and 11.0% cis-2-butene.…

    • 836 Words
    • 6 Pages
    Good Essays
  • Powerful Essays

    The objective of this experiment is to successfully perform a dehydration of 1-butanol and 2-butanol, also dehydrobromination of 1-bromobutane and 2-bromobutane to form the alkene products 1-butene, trans-2-butene, and cis-2-butene. The dehydration reactions react under and acid-catalysis which follows an E1 mechanism. It was found that dehydration of 1-butanol yielded 3.84% cis-2-butene, 81.83% trans-2-butene, and 14.33% 1-butene, while 2-butanol is unknown due to mechanical issues with the GC machine. For the dehydrobromination, with the addition of a strong base that can abstract a proton, which then pushes off the leaving group and a new sigma bond makes a new π-bond all at one time, this is follows E2 mechanism. It was found that the dehydrobromination of 1-bromobutane yielded 100% 1-butene, while 2-bromobutane yielded 13.09% cis-2-butene, 49.95% trans-2-butene, and 36.97% 1-butene.…

    • 1583 Words
    • 7 Pages
    Powerful Essays
  • Satisfactory Essays

    6. Add 2.24 grams of iron filings a little at a time to the hot solution. Allow the beaker to cool for 10 minutes.…

    • 228 Words
    • 3 Pages
    Satisfactory Essays
  • Good Essays

    4) Transfer measured acid solution to a flask and add 3 drops of phenolphthalein and sodium hydroxide solution while stirring.…

    • 920 Words
    • 5 Pages
    Good Essays
  • Good Essays

    3 Isomers of butanol

    • 1021 Words
    • 5 Pages

    An alcohol's reactivity is determined based on the attachment of their hydroxyl functional group. The location of this hydroxyl functional group will impact the molecular structure of the alcohol, making it either primary (1° ), secondary (2° ), or tertiary (3° ). The purpose of this experiment is to observe and predict the reactions that take place between all three alcohols and an oxidizing agent, as well as to test our theories of how the molecular structure affects the chemical properties of the three isomers of butanol.…

    • 1021 Words
    • 5 Pages
    Good Essays
  • Powerful Essays

    The synthesis of the alkyl halide n-Butyl Bromide from alcohol is the foundation for the experiment. During the isolation of the n-butyl bromide, the crude product is washed with sulfuric acid, water, and sodium bicarbonate to remove any remaining acid or n-butyl alcohol. The primary alkyl halide halide n-butyl bromide is prepared by allowing n-butyl alcohol to react with sodium bromide and sulfuric acid. The sodium bromide reacts with sulfuric acid to produce hydrobromic acid . Excess sulfuric acid acts to shift the equilibrium and speed up the reaction by producing a higher concentration of hydrobromic acid. The sulfuric acid protonates the hydroxyl group of n-butyl alcohol so that water is displaced instead of the hydroxide ion OH-. The acid also protonates the water as it is produced in the reaction and deactivates it as a nucleophile. Deactivation of water keeps the alkyl halide from being transformed back to the alcohol by nucleophilic attack of water. The reaction of the primary substrate continues via an SN2 mechanism.…

    • 1598 Words
    • 7 Pages
    Powerful Essays
  • Good Essays

    Sn1 Sn2 Reactions

    • 1979 Words
    • 8 Pages

    The purpose of this experiment is to synthesize 1-bromobutane from 1-butanol and sodium bromide. In order for this reaction to reach completion there are four major operations that need to be performed. The four major operations include refluxing, simple distillation, separation, and drying.…

    • 1979 Words
    • 8 Pages
    Good Essays
  • Satisfactory Essays

    Through this experiment, I determined the relative rates of reactions of several alkyl bromides under SN1 and SN2 conditions. Through careful analysis, I was able to determine the relative rates of reactions of several alkyl bromides. My results do not match my predictions. The differences between my predictions from the results I observed, for the NaI/acetone test, include: 2-Bromo-2-methylpropane was the third compound to react, where I had it as the first compound to react, and 1-Bromobutane was the first compound to react, where I had it as the third compound to react. The differences between my predictions from the results I observed, for the AgNO3/ethanol test, include: 1-Bromobutane was the first compound to react, where I had it as…

    • 250 Words
    • 1 Page
    Satisfactory Essays
  • Better Essays

    Synthesis of 1-Bromobutane

    • 3050 Words
    • 13 Pages

    The purpose of this experiment is to synthesize 1-bromobutane from 1-butanol and sodium bromide. In order for this reaction to reach completion there are four major operations that need to be performed. The four major operations include refluxing, simple distillation, separation, and drying.…

    • 3050 Words
    • 13 Pages
    Better Essays
  • Satisfactory Essays

    Vinegar Titration

    • 424 Words
    • 2 Pages

    2. Pipet one 10.00mL portion into a clean 100mL volumetric flask and dilute to the mark.…

    • 424 Words
    • 2 Pages
    Satisfactory Essays
  • Powerful Essays

    Objective: The purpose of this lab is to prepare 1-bromobutane from 1-butanol in an acid-catalyzed substitution reaction. While the reaction would be expected to occur as SN2 due to the primary nature of the substrate, because H2SO4 is used as a solvent, the conditions are very polar and the reaction can proceed via an SN1 reaction. The main objective is to obtain test results to determine the mechanism of the reaction and purity of the product.…

    • 1544 Words
    • 7 Pages
    Powerful Essays
  • Good Essays

    Substitution Reactions of 3-phenyl-1-phenol, 2-pentanol, and 2,4-dimethyl-3-pentanol Samantha Sparks, Isi Nosegbe and Sabrina Becker. Department of Chemistry, IUPUI, 402 N. Blackford St., Indianapolis, IN 46202 This project was collaborated on by three different organic chemistry students, who individually synthesized and researched each of the three substitution reactions in this experiment.. The first reaction was an Sn2 reaction of 3-phenyl-1-propanol with NaBr and H2SO4 to create1-bromo-3-phenylpropane. Though multiple trials were ran no successful results of reaction one were obtained.…

    • 1027 Words
    • 5 Pages
    Good Essays
  • Better Essays

    2. The alcohol was poured in a separating funnel the mass of measuring cylinder was recorded. 25cm3 of concentrated HCl was added into the funnel in 10 portions. After each addition, the funnel was closed and inverted several times. The switch was opened for releasing pressure.…

    • 1561 Words
    • 7 Pages
    Better Essays
  • Good Essays

    (4) To carry out the preparation of solutions of desired concentration from more concentrated solution…

    • 806 Words
    • 4 Pages
    Good Essays