Aldehyde and Ketone 1. ALDEHYDE Definition: An aldehyde is an organic compound containing a formyl group. This functional group‚ with the structure R-CHO‚ consists of a carbonyl center (a carbon double bonded to oxygen) bonded to hydrogen and an R group‚ which is any generic alkyl or side chain. The group without R is called the aldehyde group or formyl group. Aldehydes differ from ketones in that the carbonyl is placed at the end of a carbon skeleton rather than between two carbon atoms
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This is a list of currently emerging technologies‚ which contains some of the most prominent ongoing developments‚ advances‚ and innovations in various fields of modern technology. Emerging technologies are those technical innovations which represent progressive developments within a field for competitive advantage.[1 In the history of technology‚ emerging technologies are contemporary advances and innovation in various fields of technology. Various converging technologies have emerged in the
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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 1‚4-Dimethoxybenzene‚ and then determine the percent yield and
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The Role Catalysts In Chemical Reactions‚ Their Importance In Industry‚ Problems and New Developments OXFORD AND CAMBRIDGE SCHOOLS EXAMINATION BOARD. General Certificate Examination - Advanced Level Chemistry (Salters’) - Paper 3 mock. ROBERT TAYLOR U6JW. A Catalyst is a substance that alters the rate of a reaction. The catalyst remains unchanged at the end of the reaction. The process is called catalysis. In this report I aim going to explain the role of catalysts in chemical reactions and their
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Functional Group Analysis: Carbonyl Compounds‚ Oxidizable Carbonyl Compounds and Acidic Compounds Christian Paul L. Ramos Institute of Chemistry‚ University of the Philippines‚ Diliman‚ Quezon City 1101 Philippines Date Performed: August 24‚ 2012; Date Submitted: September 19‚ 2012 Results and Discussion Aldehydes and ketones both contain the carbonyl group – a group in which a carbon atom has a double bond to oxygen. The carbonyl group in aldehydes is bonded to at least one
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CONCEPTS IN ORGANIC CHEMISTRY • Inductive Effect : Inductive effect is defined as permanent displacement of shared electron pair in a carbon chain towards more electronegative atom or group. Types of Inductive effect : 1.Negative Inductive Effect : (—I effect‚ Electron withdrawing effect) when an electronegative atom or group (more electro negative than hydrogen)is attached to the terminal of the carbon chain in a compound‚ the electrons are displaced in the direction of the attached
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Friedel-Crafts liquid phase alkylation reaction of aromatic compounds is an industrially important which is known since 1877 and also commonly practiced in organic chemistry for the synthesis of various pharmaceutical compounds [1]. Catalytic benzylation of aromatics with benzyl chloride is one of the commercially significant C-C bond synthetic reaction processes to produce benzylated aromatics such as diphenylmethane and substituted diphenylmethanes. These are key intermediates in the synthesis
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[19593 Organic Chemistry of the Tramition Elements. Part r. View Online 551 Downloaded by University of Washington on 01 February 2011 Published on 01 January 1959 on http://pubs.rsc.org | doi:10.1039/JR9590000551 113. The Organic Chemistry of the Transition Elements. Part I. Tricarbonylchromium Derivatives of Aromatic Compounds. By B. NICHOLLS M. C. WHITING. and Many aromatic compounds‚ ArH‚ displace carbon monoxide from chromium hexacarbonyl with the formation of complexes Cr(CO)
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Chemistry : Important Questions For CBSE Class XII ( Haloalkanes and Haloarenes) (Q.1) Choose the incorrect statement about the benzyl chloride: ( 1 mark ) (a) It is less reactive than alkyl halides. (b) It can be oxidized to benzaldehyde by boiling with copper nitrate solution. (c) It is a lachrymatory liquid and answers beilstein’s test. (d) It gives a white precipitate with alcoholic silver nitrate (Q.2) Dry ether The reaction RX + 2Na + RX _______________? R-R + 2NaXis called. ( 1 mark
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Abstract A Friedel-Crafts alkylation was performed by adding t-butyl alcohol to p-dimethoxybenzene in order to produce 1‚4-di-t-butyl-2‚5-dimethoxybenzene. This reaction yielded 0.009g of 1‚4-di-t-butyl-2‚5-dimethoxybenzene having a percent yield of 5%‚ and a melting point range of 54.8°C-56.9°C. Introduction This reaction is designed to put functional groups onto aromatic rings. This is done through an electrophilic aromatic substitution where a positive species is strong enough to pull electrons
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