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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+3. Complete the chemical equations for the following reactions. Draw the structure (condensed structural formulas) for the dominant product and write the names of the reactants and products (organic compounds only.) d) CHy Name reactant: Name product: e) CH=C-CH + 2 HBr 4-Cて。 Name reactant: Name product:How to synthesize 1-phenyl-1-bromopropane from benzene?
- Write the chemical equation for the reaction of ethanoic acid with N-methylethanamine. Which is formula of this rule of reaction?What functional groups are present in: m-nitroanline? n,n-dimethyl aniline? cholesterol? palmitic acid? napthalene? Please list all. I have 2 benzene groups for napthalene. Palmitic Acid: 15-carbon alkane and carboxylic group N,N-dimethyl aniline:amine and phenol Cholesterol: alcohol and alkene M-nitroaniline; amide but not sure what else. Please help. Thank you.12) Synthesize 2-methyl-prop-2-enal from organic precursors with 2 or fewer carbons and inorganic precursors.
- 4.) HX is used as a reagent in the reaction below. „NH2 он + HX + :NEN: + A. What functional-group transformation occurs in this reaction?The acid-catalyzed dehydration of 2,3-dimethyl-3-pentanol yields three alkene products. What are the names of the three alkenes? Which of the three alkenes is the major product?SN2 reaction is an example of a nucleophilic substitution reaction. Imagine that 1-iodobutane reacts with 4-methylheptan-1-ol under basic conditions. Draw the structure of the two reactants.