Experiment VI: Oxidation of Isoborneol with Bleach 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. Procedure: Using a 50-mL Erlenmeyer flask‚ 1.316 g (8.5 mmol) isoborneol and 1.0 mL (17 mmol) glacial acetic acid were stirred vigorously with a magnetic stir plate. A volume of 1.7 mL NaOCl
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Oxidation of Borneol to Camphor Objectives: The purpose of this experiment was to use oxidation to convert (1S)-(-)-borneol into (1S)-(-)-camphor‚ which was done via the use of reagents such as glacial acetic acid and sodium hypochlorite and laboratory techniques learned in previous labs. Afterward‚ the final desired product was obtained‚ and to characterize and ensure the purity of the product‚ further lab techniques were implemented. Overall Reaction: 0 out of 10 Oxidation Reaction:. Mechanism:
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Borneol; An Oxidation-Reduction Scheme Nicolas Gibson Lab Time: Tuesday 11:30 am Abstract: In this experiment‚ the main objective was to synthesize a ketone from borneol via an oxidation reaction and secondly‚ to produce a secondary alcohol from camphor via a reduction reaction. Therefore‚ the hypothesis of this lab is that camphor will be produced in the oxidation reaction and isoborneol will be the product of the reduction reaction because of steric hindrance. For the oxidation
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the experiment was to perform a reduction reaction on the ketone group of camphor to the OH group on isoborneol. In order to successfully synthesis the reactant to the product‚ NaBH4 was used as the main reagent to reduce the carbonyl double bond. One believes the formation of isoborneol was successfully due to the product’s percent yield‚ IR‚ and melting point. During the lab‚ .077 grams of isoborneol was yielded from the camphor reduction. In result‚ .077 g compared to an theoretical yield of .102
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Title : reduction of camphor to isoborneol Hend Altajjar Date: 01\30\2015 disk no. 116 lab report experiment procedure I scaled up 0.120 g of camphor ‚ the I added 1.0 ml of methanol in a 10-ml Erlenmeyer flask. I stirred with a glass stirring rod until the camphor has dissolved. Then I
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Title: The Green Oxidation of Borneol to Camphor Date Conducted: February 8‚ 2012 April 27‚ 2012 Abstract: The goal of this experiment was to perform a Green Oxidation of Borneol to Camphor‚ without the use of Chromium synthesis since it is toxic to the environment. Reagent Table: |Chemical Name |Amount used |Molecular weight |Concentration |Density g/mL |BP °C |MP °C |Chemical Formula
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“oxidized”. These reactions can be carried out in lab‚ or they can occur naturally via oxidants or reductants—substances that have the ability to oxidize or reduce other substances‚ respectively. Theory‚ Reactions‚ and Mechanisms In this lab‚ Borneol will be oxidized to camphor in a common reaction known as the Jones Oxidation Reaction. It is true that oxidation reactions subtract electrons‚ lowering its oxidation state. However in organic chemistry‚ a more detailed explanation of the oxidation
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Introduction: Borneol (FIGURE-1)‚ first reported and published in the Tang Bencao in 659 A.D.‚ is often used in drug treatment‚ especially in Chinese drugs. It is helpful in opening obstruction of orifices‚ heat syndromes and pain releasing (Dharmananda). Nowadays artificially synthesized borneol‚ a mixture of borneol and isoborneol (FIGURE-2)‚ becomes more popular than pure natural borneol because of the lower cost in drug production. However‚ isoborneol is more toxic than borneol and thus is not
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impossible to reach‚ and 10C-15C variation is acceptable. Questions 1). The infrared reading comparison between camphor and borneol+isoborenol is that camphor does not have a OH-stretch at 3400‚ but it does have a C=O stretch around 1700-1750 that borenol and isoborneol doesn’t have. The IR readings of isoborneol and borneol look very similar the major difference is that isoborneol has a higher intensity reading from the 1500-1000 wavenumbers. 2). The peaks are different due to the position of the
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(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
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