What is the background on the chemistry of electrophilic aromatic substitution reactions, what is the importance of nitration reactions in organic synthesis, and the reactivity of methyl benzoate, a methyl ester of benzoic acid. With references
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- 3) Draw equations of the following reactions and and explain to which direction is the respective quillibrium shifted. a) cyclohexylamine + water b) aniline + sulphuric acid c) triethylamine + acetic acidwhen acetic acid is reacted triethylamine, an acid-base reaction occurs. Write a detailed mechanisim for this reaction. Provide all reasonable resonance forms for the product.Carboxylic acids do not give characteristic reactions of carbonyl group. Explain why?
- Oo.139. Subject :- ChemistryHeterocyclic compounds are present in naturally occurring substances and their syntheticcompounds are produced for various industrial applications. Furan is one such heterocycliccompound which is more reactive than benzene towards electrophilic aromatic substitutionreaction.1.Analyze the different substitution products formed in case of furan when it is reacted withiodine. Write the reaction mechanism involved when furan reacted with iodine andevaluate the formation of products.I need a detailed diagram or table of every reaction in organic of: alcohol, aldehyde, ketone, epoxide, ester, ether, amide, anhydride, carboxylic acid, and functional derivatives of carboxylic acid. How to go from one to another, and the elaborated cycle of the reactions
- 1. Arrange the following compounds in order of increasing acidity and explain the reason for the arrangement: Ethanoic acid, Butanoic Acid, Benzoic Acid, Salicyclic acid. 2. Arrange the test samples in order of increasing reactivity with sodium bicarbonate? Explain briefly. -Ethanoic acid, Butanoic acid, Benzoic acidV) Outline a synthesis of the following compound from benzene and other appropriate organic or inorganic reagents. ? CH3 ? CO2H Excess ?.4 D.3 QUESTION 20 As learned in the synthesis of 1-bromo-3-chloro-5-iodobenzene, electron donating groups enhance the reactivity of benzene towards electrophiles, and electron withdrawing groups decrease the reactivity of benzene towards electrophiles. Based on this, which of the following benzene derivatives is the LEAST REACTIVE towards electrophiles? NO2 NH2 O A. 3 O B. 4 OC 1 O D.2 Click Save and Submit to save and submit. Click Save All Answers to save all ansurers. e here to search Esc #3 8. 3. 4. R IT Q Tab G H CapsLk V B N M C Shift Alt この 7
- G.178.A- What is the definition of acidity? B- Compare the acidity of ammonia and its aliphatic derivatives with of acidity pyrrole C- Melting points of pyrrole is higher than melting point of 1-methyl pyrrole explain your answer D- Why does pyrrole prefer electrophilic substitution reactions? E- Why Pyrrole is considered to be an aromatic compound ? F- Explain the Reimer-Tiemann reaction mechanism of heterocyclic compounds? G- Why pyridine is a weak base? explain your answer? H- Pyridine can react with electrophiles, electrophilic substitution ? explain your answer ? G- Explain the Diels–Alder reaction mechanism of heterocyclic compounds? I- From a-haloketone how can you prepared flowing compounds : Imidazole Oxazole Thiazole J- compared the acidity and basicity of Pyrazole and Imidazole with Pyrrole and Pyridine ?Arrange each group of compounds in order of increasing acidity.(c) benzoic acid, o-nitrobenzoic acid, m-nitrobenzoic acid