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Indicate the products of the reaction of 2-(3-aminopropyl)cyclohexan-1-one with H2SO4. Draw the structures of the compounds.
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- 4-pyranone will readily undergo an acid-base reaction. Identify the reaction conditions that will result in the formation of an aromatic product. Then, draw the aromatic resonance product structure. Include all lone pairs in your structure. Ignore inorganic byproducts. H3O+draw the structure for this compoundDraw the formulas of the reactants and products of the reaction: 2-ethylbutanoyl bromide with excess ethylmagnesium bromide and heating the product with concentrated H2SO4.
- Indicate compound A that must react with ethylbenzene to obtain 4-ethylbenzene-1-sulfonic acid. 3-bromo-4-ethylbenzene-1-sulfonic acid.Synthesize 2-Hydroxy-2-phenylacetonitrile from phenylmethanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.2. Draw the structures of the products that would result from the following reactions. Ph Ph. (a) (c) Ph Ph co is also produced. Ph Ph (b) =0 + Ph-C=C-Ph → (d) Ph 10 Ph co is also produced. Benzyne adds to the 9, 10 position on anthracene.
- Explain this statement: Although 2-methoxyacetic acid (CH3OCH2COOH)is a stronger acid than acetic acid (CH3COOH), p-methoxybenzoic acid(CH3OC6H4COOH) is a weaker acid than benzoic acid (C6H5COOH).Explain this statement: Although 2-methoxyacetic acid (CH3OCH2COOH) is a stronger acid than acetic acid (CH3COOH), p-methoxybenzoic acid (CH3OC6H4COOH) is a weaker acid than benzoic acid (C6H5COOH).Synthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.
- Synthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.2. Write the structure of following organic compounds 2,5- dichloro-1,4-cyclohexandione o-Nitro- m-chloroethoxybenzene 2(N-phenyl) amino-l-propanol 3-Cyclopropoxy-4-Hydroxy-2-pentenal 1,3,4,5,6-pentahydroxy-2-hexanoneHow to synthesize trans-2-methylcyclohexanol from cyclohexanone?