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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Introduction In a chromatographic separation process‚ different kinds of functional groups and number of functional groups of molecules will determine the separation. Depending on what kind of solute‚ solvent‚ and adsorbent used‚ molecules will experience the interaction during dynamic equilibrium. On a TLC plate‚ capillary tube is used to transfer o- and p- hydroxyacetopheone‚ taking advantage of capillary force to make small spotting. A 30:70 ether acetate: petroleum ether is used as a solvent
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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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Abstract Introduction The acylation of the α carbon position of a carbonyl group is one of the greatest breakthroughs that has benefited chemists in organic synthesis particularly when in need of building a carbon skeleton of interest in a molecule. For one to be able perform this acylation technique‚ there are two mar approaches which are employable. The first method involves the deprotonation of the α-Carbon atom which has a pKa known to be ̴20 through the use of a strong base for instance
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by : Directorate of Education‚ Delhi SOME IMPORTANT REASONING BASED QUESTIONS OF ORGANIC CHEMISTRY 1. Chlorobenzene is less reactive than chloromethane. Ans. In chlorobenzene‚ each carbon atom of benzenering is sp2 hyridised and is electron withdrawing. Chlorine atom donates a lone pair of electron and acquire positive charge. The negative charge is delocalised on ortho and para position by resonance. C-Cl bond acquires partial double bond character and is 169 pm as compared to 17.0 pm in chloromethane
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Benzene 1 Benzene Benzene Identifiers [1] CAS number 71-43-2 PubChem 241 ChemSpider 236 UNII J64922108F EC number 200-753-7 KEGG C01407 ChEBI CHEBI:16716 ChEMBL CHEMBL277500 RTECS number CY1400000 Jmol-3D images Image 1 [2] [3] [4] [5] [6] [7] [8] [9] Properties Molecular formula CH Molar mass 78.11 g mol−1 Appearance Colorless liquid Odor aromatic‚ gasoline-like
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2009) Abstract : 2-Acetylcyclohexanone was synthesized by acylation reaction of acidic anhydride using enamine as organiocatalyst instead of a strong base‚ NaOH‚ resulting in milder reaction conditions. The reaction was conducted in toluene and direct distillation of the reaction mixture before hydrolysis was leaded to a high yield of the pyrrolidine enamine. This condition was leaded good yields (73.6%) without side reactions. Acylation gave an enol form (71.7%) and a keto form (28.3%) of 2-acetylcyclohexanone
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Chemistry 1. Explain why 0-nitrophenol has a lower boiling point than p-nitrophenol? 2. Why alkali metals used in photoelectric cells? 3. Due to which compound‚ ozone depletion is caused in Antarctica? 4. Which of the element among B‚ Al‚ C and Si :- a. Has the highest first ionization enthalpy? b. Has the most negative electron gain enthalpy? 5. c. Write the atomic number of the element present in the third period and seventeenth group of the periodic table
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With embezzlements and bank fraud to retirement delays in the country‚ it would leave Americans in a state of fragility. Things were not the best in the days when President Nixon left office. However if we look back to 42 years ago and remember our 37th President of the United States. This was most likely a memorable day for all Americans. President Nixon was in office‚ and it was time to move forward he was a very conservative man‚ that had fresh new ideas to bring political views that would win
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days. Figure 2 shows the photograph of as grown single crystal of MPN. The theoretical Bravais‚ Friedel‚ Connay and Harker (BFDH) morphological [38] method of MPN crystal with indexed (hkl) planes was determined using the unit cell and positional coordinates of MPN by MERCURY software program [39]. The MPN crystal shows well developed morphology with several habit faces‚ for each face its parallel Friedel plane is also present in the grown crystal which is shown on Figure
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