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Draw the structures of three different tautomers of xanthine.
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- Draw a structural formula of the principal product formed when ethyl benzoate is treated with reagent. Q.) LiAlH4, then H2ODraw a structural formula of the principal product formed when ethyl benzoate is treated with reagent. Q.) C6H5MgBr (two equivalents), then HCl/H2ODraw the skeletal structures of: phenyl benzoate, benanilide, benzoic acid, and 2-napthaldehyde and identify the carbonyl-containing functional group.
- What are the structures of cyclohexanone and salicylaldehyde substances constitutes? i) Is it saturated or unsaturated or aromatic amine or phenol? ii) Aromatic or Aliphatic in nature? iii) What is their functional group? (aldehyde/ketones/esters)Draw a structural formula of the principal product formed when ethyl benzoate is treated with reagent. Q.) H2O, H2SO4, heatTRUE OR FALSE; The carbonyl carbon in an amide and the carbon in an aromatic ring have the same hybridization.
- Does each of the compounds contain a carbonyl group?Complete the following syntheses – they may be two- or three-step processes. Include any necessary catalysts or reaction conditions. c) Prepare methyl ethanoate from ethanol and methanolDraw the structural formula for each of the following compounds. a) 2-amino-2,3,4-trimethyl-4-heptene Structure: b) 5-tertbutylnonane Structure: c) 3-hydroxy-2,4,6-trinitrophenol Structure: d) N-ethyl-N-methyl-3-hexanamine Structure: e) 3-oxoheptanal Structure: f) cis-1,2-dimethylcyclopentene Structure:
- Amides can be form by; Group of answer choices oxidation of ether oxidation of aldehydes and ketones reaction of carboxylic acid to alcohol reaction of carboxylic acid to amineIdentify each functional group located in the following rings. Which structure represents a lactone—a cyclic ester—and which represents a lactam—a cyclic amide?An organic compound gives a positive test with Tollen's reagent (ammoniacal silver nitrate). This impliesthat the compound is a ketone is an aromatic aldehyde can be an aliphatic aldehyde is a carboxylic acid 3. A B D