Experiment 1 :Alkanes&Alkenes:Combustion and action of sulphuric acid. Introduction In the study of organic chemistry‚ the organic compounds which are made up of carbon and hydrogen are called hydrocarbons. They can be gases as‚ propane‚ they can be liquids‚ for example‚ benzene‚ or they can be low-melting solids and waxes‚ for example‚ polystyrene. There are four classifications of hydrocarbons; saturated hydrocarbons or alkanes‚ unsaturated hydrocarbons or alkenes and alkynes‚ cycloalkanes‚ and
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Straight Chain Alkanes The general formula for an alkane is CnH2n+2 wheren is the number of carbon atoms in the molecule. There are two ways of writing a condensed structural formula. For example‚ butane may be written as CH3CH2CH2CH3 or CH3(CH2)2CH3. Rules for Naming Alkanes * The parent name of the molecule is determined by the number of carbons in the longest chain. * In the case where two chains have the same number of carbons‚ the parent is the chain with the most substituents.
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1. Explain the meaning of the term ’workplace exposure limit’. (2) The term "workplace exposure limit" (WEL) is concerned with concentrations of hazardous substances in the air that people breathe averaged over a specified period of time and referred to as a time weighted average. 2. Acute injuries normally lead to sickness leave from work and a period of rest during which time the damage heals. 3. Chronic injuries build up over a long period of time and are usually irreversible‚ producing illnesses
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Additional Mathematics Project Work 2012 Sculpture for the Additional Mathematics Corner of Sekolah Tinggi Muar‚ Johor Name : I/C No : School : Sekolah Tinggi Muar Integration Contents 1. Title : Sculpture for the Additional Mathematics Corner of Sekolah Tinggi Muar page 1 2. Appreciations:
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Experiment # 1 Date: 18/12/13 Title: Chemical Properties of Alkanes. Aim: To test the reactivity of alkanes using cyclohexane as an example. Apparatus/Materials: Cyclohexane‚ liquid alkane‚ aqueous bromine‚ test tubes‚ light source‚ watch glass‚ splint‚ 0.1 MKMnO4‚ concentrated H2SO4‚ dilute H2SO4. Method: Combustion: 1. A watch glass was placed on a benched protection sheet in a fume cupboard and the extractor in the fume on. 2. 4 drops of cyclohexane was placed on the watch glass using
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LEVEL CHEMISTRY ASSESSED HOMEWORK Answer all questions Max 86 marks Name …………………………………………………………….. Mark ……../86 ……....% Grade ……… 1. The graph below shows the boiling points of some alkanes. (a) Draw a smooth curve through the points on the graph and estimate the boiling points of octane C8H18‚ ……………… hexadecane‚ C16H34 .……………… [2] (b) State how decane‚ C10H22‚ can be separated from a mixture of the alkanes. ...............................................
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Old Dominion University ORGANIC 214 Alkene Addition Submitted by: Alkene addition: Bromination of (E) Stilbene Introduction: In this lab we used the greener approach‚ which involves the addition of bromine across a double bond. When bromine reacts with E-stilbene (trans-1‚2-diphenylethene)‚ two new chiral carbons are created from the sp2 carbons‚ therefore 3 different dibrominated stereoisomers are possible: meso-(1R‚2S)‚ or the raceminc mixture-(1R‚2R) or (1S‚2S)-dibromo-1‚2-diphenylethane
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Electrophilic Aromatic Substitution: Bromination of Aromatic Compounds Introduction: The experiment focuses on finding out what kind of activating effects that four different substituents will have on an aromatic benzene ring. The substituents being tested are aniline‚ anisole‚ acetamide (acetanilide)‚ and phenol. All four of these groups are either para or ortho activating. Bromination is the reaction that will be carried out. The melting point ranges of the final products will be taken in order
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Lab 1: Alkene Addition: Bromination of (E)-stilbene I. Introduction: 1. The purpose of the experiment was to perform an electrophilic addition reaction by using pyridinium tribromide to brominate (E)-stilbene and to identify whether it formed the meso- or racemic product through melting point analysis. 2. This is the mechanism for the bromination of (E)-stilbene. However‚ this is the mechanism for Br2 and in class we us Pyridinium Tribromide instead due to the difficulties associated
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Additional Questions – Test Strategy Table of Contents 1 Purpose 3 2 About Additional Questions 3 3 Requirements 4 3.1 As-Is and New AQ Features 4 AQ As-Is Feature from V1 4 AQ Additional / Enhanced Feature for V2 4 Create AQ functional Component 4 AQ FCA linked to Scoring FCA 4 Create AQ Event by copying an existing event (closed‚ open‚ draft & archived) 4 Invite Supplier 4 3.2 AQ High Level Functionality and List of User Stories 5 Table below gives the mapping of
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