say that a hydrocarbon is saturated‚ we mean that the carbon is saturated with other atoms. It can only bond to a new atom if it gives up one of the atoms it is already bonded to. Hydrocarbons that contain at least one double carbon bond are the alkenes and those that contain at least one triple carbon bond are called alkynes. These are compounds that are also known as unsaturated molecules. Lastly‚ aromatic‚ is a class of cyclic hydrocarbons that contain a closed loop of electrons. Generally
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D1: Pharmaceutical drugs D.1.1 List the effects of medicines and drugs on the functioning of the body. Drug or medicine is a substance that does one or more of the following: Alters physiological state – consciousness‚ activity level‚ coordination Alters incoming sensory experience Alters mood or emotion The active ingredients in drugs and medicines can be isolated from a plants and animals or synthesized artificially. Drugs supposed to assist human body’s
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of molecules. Caffeine had already existed in the leaf itself but needed to be separated from the other chemicals. Caffeine’s chemical structure is relatively similar to the nucleic acid purine in that they use nitrogen and is bicyclic but lacks an alkene‚ amine and an amide. Caffeine has a solubility of 67.0 g/100 mL in boiling water but tannins also boil in hot water to form catechin. Catechin cannot react with water but it can with calcium carbonate. The calcium carbonate was added into the reflux
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General Features of Oxidative Additions Oxidative addition reactions usually involve a coordinatively unsaturated 16-electron metal complex or five-coordinate 18-electron species‚ and take the general from: [pic] If the A and B ligands in the product are considered to be formally –1‚ then the metal center has increased its oxidation state by +2‚ and this is the origin of the name oxidative addition. Oxidative reaction can occur when a metal complex
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Nucleophilic Substitution Reactions of Alkyl Halides 1. Summary of Experiment In this experiment we will be comparing the both SN1 and SN2 reactions using various compounds and sodium iodide and silver nitrate. We will be comparing the nature of the leaving group (Cl vs Br) in the 1-halobutanes as well as the effect of the structure
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Mark Scheme (Results) Summer 2012 International GCSE Chemistry (4CH0) Paper 1C Science Double Award (4SC0) Paper 1C Edexcel Level 1/Level 2 Certificate Chemistry (KCH0) Paper 1C Science (Double Award) (KSC0) Paper 1C Edexcel and BTEC Qualifications Edexcel and BTEC qualifications come from Pearson‚ the world’s leading learning company. We provide a wide range of qualifications including academic‚ vocational‚ occupational and specific programmes for employers. For further information‚
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containing the gascous products. The brown colour of bromine water disappeared immediately. Why? The products of cracking contained unsaturated (hydrocarbons) / alkenes / C=C / ethane / reasonable name of alkene‚ which decolourised the bromine water immediately by addition reaction (2) (II) The student then dropped more bromine water into the boiling tube until the brown colour of the bromine water persisted. After about 10 minutes‚ the brown colour disappeared.
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1. A student neglected to add sodium carbonate when extracting the tea leaves with hot water. Yet a very high yield of caffeine was obtained. The crystals melted at 202-214°C. Explain. • The sodium carbonate is supposed to be added when extracting the tea leaves with hot water in order to help purify the caffeine. So since the student neglected to add sodium carbonate the caffeine won’t be pure but the student would still be able to recover a large amount of caffeine. The literature melting point
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temperature around 100C or less. The crude product was collected which contained water‚ 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
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