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 to determine their identities and reactivity. It is predicted that substitution order from most to least reactive should be aniline‚ phenol‚ anisole‚ and acetamide. Theory: Regioselectivity and the rate of electrophilic
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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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Diels-Alder Synthesis of Exo-Norbornene-cis-5‚6-Dicarboxylic Anhydride for Organic Chemistry Laboratory Instruction Kyle Myers and Dr. James Roark University of Nebraska at Kearney‚ Department of Chemistry‚ Kearney‚ NE 68849 Abstract A technique for the Diels-Alder synthesis of endo-norbornene-cis-5‚6dicarboxylic anhydride and its stereoisomer‚ exo-norbornene-cis-5‚6-dicarboxylic anhydride‚ is explained. To prove that each stereoisomer was made in the experiment and to distinguish between the
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Introduction:The purpose of this lab was to determine the activating effect of aniline‚ phenol‚ anisole and acetanilide after reacting with pyridinum tribromide in order to undergo electrophilic aromatic substitution. The melting point of the isolated products were measured against the standards in order to determine how strong of an ortho/para activator the compound was based on the product(s) and melting point obtained. Theory: Electrophilic aromatic substitution is an organic reaction that takes
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CHEMISTRY OF HYDROCARBON EXPERIMENT 16 OBJECTIVE The objective of this experiment is to distinguish the difference between various types of hydrocarbons by performing simple tests and reactions involving hydrocarbons. EQUIPMENT AND CHEMICALS Pentene Toluene Heptane Potassium permanganate (1% KMnO4) Aluminum chloride (anhydrous AlCl3) Chloroform (CHCl3) Ligroin Br2 in CCl4 (5%) Stopper pH paper Small test tubes and rack Graduated cylinder (10 ml) Evaporating dish DISCUSSION
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Chemistry GENERAL CHEMISTRY: Atomic Structure and elementary quantum mechanics: Blackbody radiation‚ Planck’s radiation law‚ photoelectric effect‚ Compton Effect‚ de Broglie’s hypothesis‚ Heisenberg’s uncertainty principle. Postulates of quantum mechanics‚ Schrodinger wave equation and a particle in a box‚ energy levels‚ wave functions and probability densities‚ Schrodinger wave equation for H-atom‚ Separation of variables‚ Radial and angular functions‚ hydrogen like wave functions‚ quantum numbers
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The alkylation of 1‚4-dimethoxybenzene is very favorable because of the presence of two methoxy groups. The groups act as activators to electrophilic aromatic substitution because of their ability to donate electrons through resonance. This enhanced activation helps favor the initial substitution. After this‚ the ring has two methoxy groups and an alkyl group attached to it. The addition of the alkyl group further activate the ring for another electrophilic aromatic substitution. The addition of
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Br2/HBr solution‚ the products were crystallized and melting points attained to verify relative reactivity. My assignment‚ 2‚4-Dibromoanisol‚ was prepared in a yield of 52% with a melting point of 55-58 C . Reaction: Mechanism: Procedure: Anisole (0.35mL‚ 0.0378mol) was obtained and placed in a pre-weighed 25 mL round bottom flask‚ along with 2.5 mL of glacial acetic acid and a magnetic stir bar. Then the reaction apparatus was assembled‚ the dry tube was charged with conc. sodium bi sulfate
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163 CHAPTER 13 HYDROCARBON Hydrocarbons are composed of Carbon and hydrogen. The important fuels like Petrol‚ kerosene‚ coal gas‚ CNG‚ LPG etc. are all hydrocarbons or their mixture. Sources: Petroleum and natural gas are the major sources of aliphatic hydrocarbon while coal is an important source of aromatic hydrocarbons. The oil trapped inside the rocks is known as petroleum. PETRA – ROCK‚ OLEUM – OIL. The oil in the petroleum field is covered with a gaseous mixture known as natural
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