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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9.3 – The Acidic Environment: Δ. Construct word and balanced formulae equations of all chemical reactions as they are encountered in this module: NOTE: In chemistry‚ [x] means “concentration of x” in moles per litre (mol/L). EG: [H3O+] means “concentration of H3O+ ions” in mol/L. BASIC reactions to remember: Acid reactions: acid + base salt + water acid + metal salt + hydrogen gas acid + carbonate carbon dioxide gas + salt + water Formation of hydronium: H+ + H2O H3O+ Reactions of
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OCR gateway Core C1 revision notes Anything written in purple is for higher tier Exam tips are in red Fossil Fuels 3 types Coal (made from dead plants that lived millions of years ago) Crude oil (made from dead sea creatures that lived millions of years ago) Natural gas (made from dead sea creatures that lived millions of years ago) Key words to learn Non-renewable- fossil fuels are said to be this as we are using them up faster than they can be made Finite- these will run out if we
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Classification for Functional Groups Alcohols Lucas test (Differentiates primary‚ secondary‚ and tertiary alcohols) Reagent: ZnCl2 in conc. HCl Observation: Rate of reaction (tertiary alcohol> secondary alcohol> primary alcohol) Procedure: 2mL Lucas Reagent in test tube+ 3-4 drops of alcohol‚ stopper‚ shake vigorously‚ NOTE time required (less than 10m mins only) to form an emulsion or separate layers. Oxidation (Confirms if alcohol is oxidizable: presence of H in C-OH bond) Reagent:
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Contents PART XV ANALYTICAL CHEMISTRY Chapter 63 Detecting the presence of chemical species Action of heating solid sample strongly 1 Chapter 64 Separation and purification methods Centrifugation Sublimation Partition equilibrium of a solute between two immiscible solvents Two-dimensional thin-layer chromatography 2 2 3 6 Chapter 65 Quantitative methods of analysis Detection of end point in acid-alkali titration 8 Chapter 66 Instrumental analytical methods More
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acetate via Fischer esterification reaction between acetic anhydride and isoamyl alcohol‚ using concentrated sulfuric acid as a catalyst. This reaction is characterized by the combining of an alcohol and an acid (with an acid catalyst) to yield and ester plus water. In order to accomplish this reaction‚ the reactants were refluxed for 30 minutes at 80 degrees Celsius ‚to yield a mixture‚ the mixture was then mixed with sodium hydrogen carbonate and dried with anhydrous sodium sulfate. The product obtained
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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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Synthesis of Phenols You can prepare phenols in large quantities by the pyrolysis of the sodium salt of benzene sulfonic acid‚ by the Dow process‚ and by the air oxidation of cumene. Each of these processes is described below. You can also prepare small amounts of phenol by the peroxide oxidation of phenylboronic acid and the hydrolysis of diazonium salts. Pyrolysis of sodium benzene sulfonate In this process‚ benzene sulfonic acid is reacted with aqueous sodium hydroxide. The resulting salt
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HKDSE CHEMISTRY – A Modern View (Chemistry) Experiment Workbook 5 Suggested answers Chapter 52 Importance of industrial processes Chapter 53 Rate equation Experiment 53.1 Determining the rate equation of a reaction using method of initial rate (A microscale experiment) 1 Chapter 54 Activation energy Experiment 54.1 Determining the activation energy of a chemical reaction 3 Chapter 55 Catalysis and industrial processes Experiment 55.1 Investigating the action of a catalyst 6 Experiment
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sebacoyl chloride with the loss of HCl via nucleophilic substitution. Cellulose triacetate was generated by mixing cotton balls and acetic anhydride with acidic condition under heating. Materials: Styrene‚ 1 M NaOH solution‚ CaCl2(s)‚ xylene‚ t-butyl peroxybenzoate‚ methanol‚ 5% aqueous solution of 1‚ 6-hexanediamine‚ NaOH(s)‚ 5% sebacoyl chloride in hexane‚ glacial acetic acid‚ concentrated H2SO4‚ cotton balls‚ acetic anhydride‚ CH2Cl2 Procedure: For the synthesis of polystyrene‚ 10 ml styrene
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