at every point where two lines meet. FUNCTIONAL GROUPS Alkanes and Cycloalkanes - An alkane is an acyclic saturated hydrocarbon that contains one or more carbon=carbon double bonds -Functional group: C-C group -General formula: CnH2n+2; n = number of carbon atoms -Structures of branched-chain alkanes are designated using line-angle structural formulas. (Ex. The five constitutional isomers of C6H14) -Cycloalkanes are alkanes that contain a ring of three or more carbons -General Formula
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first-hand investigation to compare the reactivity of an alkene with its corresponding alkane. (a) State the name of the alkene. 2002:16(a) 1 (b) Outline a procedure to compare the reactivity of this alkene with its corresponding alkane. 2002:16(b) 2 (c) Describe the results obtained from this first-hand investigation and include relevant chemical equations. 2002:16(c) 3 3 Explain why alkanes and their corresponding alkenes have similar physical properties‚ but very different
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Vegetative reproduction (vegetative propagation‚ vegetative multiplication‚ vegetative cloning) is a form of asexual reproduction in plants. It is a process by which new individuals arise without production of seeds or spores. It can occur naturally or be induced by horticulturists. Although most plants normally reproduce sexually‚ many have the ability for vegetative propagation‚ or can be vegetatively propagated if small pieces are subjected to chemical (hormonal) treatments. This is because meristematic
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Chemistry Revision Notes IGCSE Chemistry Triple Award Revision Guide Topic Introduction to chemistry Atomic Structure Structure and Bonding – Ionic Bonding Structure and Bonding – Covalent and Metallic Bonding Organic Chemistry - Alkanes Organic Chemistry – Alkenes / Addition Polymerisation Organic Chemistry – Alcohols / Condensation Polymerisation Calculations Periodic Table Reactivity Series and Metal Extraction Electrolysis Energetics Acids‚ Bases‚ Salts and Neutralisation Preparing and Analysing
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13. ORGANIC CHEMISTRY IV) ALKYNES SYNOPSIS Alkynes are commonly known as acetylenes. Acetylene is the simplest and important member of the alkyne series. • Alkynes contain – C ≡ C – • General molecular formula of alkynes is CnH2n–2 • Triple bonded carbons are ‘sp’ hybridized and greater s – character is associated with it. • Alkynes will exhibit chain‚ position and functional isomerism. • Their functional isomers are alkadienes and cyclo alkenes. • The minimum number of carbons required to exhibit
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www.igcse.at.ua ORGANIC CHEMISTRY OIL and its many useful PRODUCTS The origin of oil Crude oil is formed from organic material of the remains of plant and animal organisms that lived millions of years ago. These remains form sediments eg at the bottom of seas‚ and become buried under layers of sedimentary rock. They decay‚ without air (oxygen)‚ under the action of heat and pressure to form crude oil over millions of years. It is a fossil fuel because it is formed from
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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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N10/4/CHEMI/SP2/ENG/TZ0/XX 88106105 CHEMISTRY STANDARD LEVEL PAPER 2 Thursday 11 November 2010 (afternoon) Candidate session number 0 1 hour 15 minutes 0 INSTRUCTIONS TO CANDIDATES • • • • Write your session number in the boxes above. Do not open this examination paper until instructed to do so. Section A: answer all of Section A in the spaces provided. Section B: answer one question from Section B. Write your answers on answer sheets. Write your session number
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University of Maryland‚ College Park Department of Chemistry and Biochemistry CHEM 231: Organic Chemistry I‚ Fall 2014 The Highlights Bonnie Dixon TA: Courney Love Office: CHM 2130 email: bdixon1@umd.edu email: clove@umd.edu When/Where: Lecture MWF 9 a.m. – 10 a.m. in CHM 1407 Discussion T/H at 12:30 pm‚ 2 pm‚ and 3:30 pm in the CHM 1228 Course Materials: Organic
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Title : Properties of hydrocarbon Objective : 1) To study the properties of hydrocarbons. 2) To determine the unknown samples. Results : Part A : Combustion Compounds Observations Hexane There was orange flame and burned mildly during the burning process. No soots and smoke were produced. C6H14 + 19/2 O2 6CO2 + 7H2O Cyclohexene Orange flame burned vigorously. A small amount of black soot and smoke were produced during the burning process.
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