"Cyclohexanol to cyclohexanone" Essays and Research Papers

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    125mL Erlenmeyer flask it contained 20.0 mL of deionized water and 20mL of concentrated sulfuric acid was added carefully with some swirling in between. The diluted acid was cooled with an ice water bath to 20-25ºC. to the cooled sulfuric acid cyclohexanol was added carefully and slowly with swirling as well. The reaction mixture cooled 65% sulfuric acid was transferred to the 100mL round-bottomed flask through a glass funnel‚ three boiling stones were added to the mixture and the distillation started

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    General Topics

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    3168‚ Australia Received 13 October 1998; received in revised form 22 December 1998; accepted 23 December 1998 Abstract The oxidation products of cyclohexene "nd several applications as intermediates for the manufacture of useful chemicals like cyclohexanol‚ cyclohexenol/cyclohexenone‚ cyclohexadiene‚ etc. The uncatalysed oxidation of cyclohexene with molecular oxygen was studied in a batch reactor. The products‚ cyclohexene hydroperoxide‚ cyclohexenol‚ cyclohexenone and cyclohexene oxide were realised

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    Alkenes and Ketones

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    Notes Aldehydes and Ketones The major similarity between an aldehyde and a ketone is the carbonyl group. A carbonyl group is a carbon atom doubly bonded to an oxygen atom. [pic] Both molecules have a carbonyl group‚ the difference the number of carbons bonded to the carbonyl carbon. An aldehyde will have none or one and a ketone will have two carbons. All aldehydes‚ except formaldehyde‚ will have a hydrogen atom on one side of the carbonyl carbon and at least on carbon on the other side

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    Abstract Introduction The acylation of the α carbon position of a carbonyl group is one of the greatest breakthroughs that has benefited chemists in organic synthesis particularly when in need of building a carbon skeleton of interest in a molecule. For one to be able perform this acylation technique‚ there are two mar approaches which are employable. The first method involves the deprotonation of the α-Carbon atom which has a pKa known to be ̴20 through the use of a strong base for instance

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    4-methylcyclohexene‚ and trace acid. D. Questions: 1. Outline a mechanism for the dehydration of 4-methylcyclohexanol catalyzed by phosphoric acid. 2. What major alkene product is produced by the dehydration of the following alcohols? a. Cyclohexanol Cyclohexene b. 1-Methylcyclohexanol methylcyclohexene c. 2-Methylcyclohexanol methylcyclohexne d. 2‚2-dimethylcyclohexanol 1‚2-dimethylcyclohexene 3. Compare and interpret the infrared spectra of 4-Methylcyclohexene and 4-Methylcyclohexanol

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    peak at about 3300 in the IR corresponds to the O—H group in the product. The peaks to the right of aro0und 3000 are C—H related‚ those about 1599 are C—H bends‚ and the peaks at 1000-1350 are C—O related. The most plausible product seems to be cyclohexanol with a molecular formula of C6H12O. 2. Describe the stereochemical relationship between each pair of isomers. (a) Same

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    Methoxetamine Research Paper

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    Phenomenon of new drugs on the Internet: the case of ketamine derivative methoxetamine On the basis of the material available both in the scientific literature and on the web‚ this paper aims to provide a pharmacological‚ chemical and behavioural overview of the novel compound methoxetamine. This is a dissociative drug related to ketamine‚ with a much longer duration of action and intensity of effects. A critical discussion of the availability of information on the web of methoxetamine as a

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    by : Directorate of Education‚ Delhi SOME IMPORTANT REASONING BASED QUESTIONS OF ORGANIC CHEMISTRY 1. Chlorobenzene is less reactive than chloromethane. Ans. In chlorobenzene‚ each carbon atom of benzenering is sp2 hyridised and is electron withdrawing. Chlorine atom donates a lone pair of electron and acquire positive charge. The negative charge is delocalised on ortho and para position by resonance. C-Cl bond acquires partial double bond character and is 169 pm as compared to 17.0 pm in chloromethane

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    Competitive Nucleophiles

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    Katie Smith April 11‚ 2013 Competitive Nucleophiles Introduction The purpose of this experiment was to compare the nucleophilicities of chloride and bromide ions toward the n-butyl and t-pentyl alcohols. We were able to analyze this by using refractometry to measure the amounts of alkyl chloride and alkyl bromide in each reaction. Experiment Scheme (Procedure A) To begin the experiment‚ we assembled a reflux apparatus in the fume hood with a 100 mL round bottom flask and a condenser

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    organic chemistry lab manual

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    NORTHERN CARIBBEAN UNIVERSITY DEPARTMENT OF BIOLOGY‚ CHEMISTRY and ENVIRONMENTAL SCIENCE LABORATORY MANUAL Instructor: Dr. M. Wilson CHEM401: BIOCHEMISTRY for NURSES Prepared by: Oreane Collins CHEMISTRY LABORATORY REGULATIONS AND SAFETY PRECAUTIONS Reference: http://www.sciencebyjones.com/safety_rules.htm Thanks to the Flinn Scientific Safety Rules for much of the below.  General Guidelines  1. Conduct yourself in a responsible manner at all times

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