Formalin – positive * Glucose – positive * Benzaldehyde * Acetone * Sodium Nitroprusside Test – Test for presence of acetone * -Wine red solution * Iodoform Test – Test for Methyl Ketones * Acetone – positive * Ethyl methyl ketone – positive * Ethyl acetate * Special test for Benzaldehyde * Formation of crystals * Molisch Test – General test for Carbohydrates * Violet ring (2nd layer) * Glucose
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CHM456 ORGANIC CHEMISTRY 1 LABORATORY Contact hours: 3 hours/week Laboratory textbook: Pavia‚ Lampman‚ Kriz and Engel‚ Introduction to Organic Laboratoy Techniques 3rd Edition (2011) ** Students MUST obtain a copy of the textbook Synopsis This is an organic chemistry practical course which reinforce the theory and concepts studied in Organic Chemistry 1 (CHM456). It covers the learning of simple laboratory techniques such as reflux‚ distillation‚ extraction‚ crystallization and melting point
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BACHELOR OF SCIENCE (HONS) BIOTECHNOLOGY YEAR 1 SEMESTER 1‚ 2 & 3 UDBB 1164 FUNDAMENTAL ORGANIC CHEMISTRY 0 EXPERIMENT 1 PROPERTIES OF HYDROCARBONS Introduction Hydrocarbons are compounds which contain only carbon and hydrogen‚ can be classified into several types‚ depending on their structure. Aliphatic hydrocarbons are divided into three classes: alkanes (e.g. methane‚ ethane and propane) have only single bonds‚ and are said to be saturated; alkenes (e.g. ethene and propene)
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UNIVERSITI TEKNOLOGI MARA COURSE INFORMATION Confidential Code Course Level Credit Hours Contact Hours : : : : : CHM 556 Organic Chemistry II Degree 4 3 hr (Lecture) 3 hr (Practical) 3 Core CHM 456 Part Course Status Pre-requisite : : : Course Outcomes : Upon completion of this course‚ students should be able to: 1. Determine functional groups present in organic compounds using Infrared Spectroscopy and interpret Nuclear Magnetic Resonance spectra and relate the information to structural
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Nitration of Methyl Benzoate Purpose: The purpose of this experiment was to synthesize methyl m-Nitrobenzoate from methyl benzoate‚ concentrated HNO3‚ and concentrated H2 SO4 by an electrophilic substitution reaction. The H2 SO4 and the HNO3 were initially combined to form nitronium ion which was then used as an electrophile in the reaction. Crystals that were collected after the formation of the methyl m-Nitrobenzoate were collected by vacuum filtration and the product was isolated and purified
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Lab 6: Electrophilic Aromatic Substitution(1) Nitration of Methyl Benzoate(2) Synthesis of 1‚4-Di-t-butyl-2‚5-dimethoxybenzene byFriedel-Crafts Alkylation of 1‚4-DimethoxybenzenePurpose1)To carry out the nitration of methyl benzoate‚ and then identify the major product formed (position at which nitro-group substitution takes place) by thin-layer chromatography (TLC)‚ the percent yield and the melting point range. 2)To synthesize 1‚4-Di-t-butyl-2‚5-dimethoxybenzene by Friedel-Crafts Alkylation of
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refluxing began and ended once the bromobenzene addition was completed. The second phase of the experiment involved the reaction of the phenylmagnesium bromide with assigned carbonyl compound. Appropriate amounts of benzaldehyde‚ benzophenone‚ or methyl benzoate based on the amount of bromobenzene used should be added to a dry beaker along with anhydrous diethyl ether. The mixture was poured into the addition funnel‚ added to round bottom flask drop wise‚ allowed to reflux for an additional 15 minutes
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Introduction: The theory behind the extraction of a solution containing benzoic acid‚ cellulose‚ and methyl orange involves many components pertaining to the fundamental ideas of solubility and polarity. Using the concepts of like dissolving like and acid base reactions‚ a solution of organic acid (benzoic acid)‚ a water soluble compound cellulose‚ and an organic soluble compound methyl orange‚ can be separated and benzoic acid can be isolated by a method of extraction. At the fundamental
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Observations * all literature values were obtained at www.sigmaaldrich.com Chemical Volume (mL) Mass (g) Density (g/mL) Molecular Weight (g/mol) Methyl-3-nitrobenzoate - 0.1178 - 181.15 Methyl benzoate 2.00 - 1.088 136.00 Sulfuric Acid 0.60 - 1.840 98.08 Nitric Acid 0.15 - 1.510 63.01 Chemical MP Exp. (°C) MP lit (°C) Methyl-3-nitrobenzoate 72.6-75.7 78.0-80.0 Mmole Calculations: HNO3 (16M)- 0.15 mL* (0.016 mole/mL) = 0.0024 mole* (1000 mmol/mole) = 2.4 mmoles
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Triphenylmethanol Aim The aim of this experiment was to prepared Grignard reagent (phenylmagnesium bromide) from bromobenzene and magnesium‚ to use the reagent prepared to synthesise a tertiary alcohol (triphenylmethanol) by reacting reagent and ester (methyl benzoate)‚ and the product formed is analyse by infrared spectroscopy (IR)‚ melting point‚ thin layer chromatography (TLC)‚ gas chromatography mass spectrum (GCMS) and finally Nuclear Magnetic Resonance spectroscopy. Introduction Formation of long hydrocarbon
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