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- Citronellol ((3R)-3,7-dimethyloct-6-en-1-ol, C10H20O) is an organic fragrance found in the oil extracted from lemon grass. a) Name the two functional groups present in the molecule. b) When a few drops of bromine dissolved in hexane is added to a sample of citronellol the brown colour of the bromine rapidly disappears. i. What type of chemical reaction has occurred? ii. Draw the structure of the product formed. iii. Name the product. c) The product formed when citronellol is heated with a mixture of potassium dichromate and sulfuric acid gives a yellow/orange precipitate when shaken with Brady’s reagent (2,4-dinitrophenylhydrazine). It also shows a positive result with Fehling’s solution. i. What type of chemical reaction has occurred ? ii. What type of functional group is present in the product? d) Explain the type of stereoisomerism which may occur in citronellol.Draw the structure for the following compound. (3R,5S,6R)-5-ethyl-3,6-dimethylnonanedraw the structure(s) of the major organic product(s)
- What two enamines are formed when 2-methylcyclohexanone is treated with (CH3)2NH?▼ Part A Name the following compound. CH,CH,CH,CH3 CH₂CH₂CC CH CH₂CH₂CH3 O 3-ethyl-3-propyl-1-heptyne O 3-butyl-3-propyl-4-pentyne O 5-ethyl-5-propyl-6-heptyne O 3-butyl-3-propyl-1-butyne O 3-butyl-3-propyl-1-pentyne Submit Request Answer Provide FeedbackWhat is the IUPAC name of the following compounds?
- No explanantion or anything needed just draw the compounds in organic chemc) rite in the reagent(s) over the arrow. a) C6H5N₂+ b) C6H5C=N H3C- An OH H₂C → benzene H3C benzylamine CI CH3Compound A has molecular formula C6H12. Upon treatment with NBS and irradiation with UV light, exactly two constitutional isomers are formed. Which of the following is a possible structure for compound A? OI Oll O III OI and II I and III || |||
- 1) Provide the name for each structure shown. NO ₂ 2) Draw the structure of the molecule with the following name: a) (1R, 3S)-Cyclopent-4-ene-1,3-diol b) (2R, 3Z)-3-Chloro-2phenylhex-3-enal c) (2E,4Z)-Hepta-2,4,6-trienoic acid d) (3R, 4E)-3-isopropyl-6-oxohex-4-enenitrile H₂C NH CH3 CH3 H₂N CH3Which hydrogenation would convert but-2-yne to (Z)-but-2-ene? A) Na/NH3 B) H₂, Pt C) Lindlar's Catalyst Which hydrogenation would convert but-2-yne to (E)-but-2-ene? A) Na/NH3 B) H₂, Pt C) Lindlar's Catalyst30. Name the following compound using systematic IUPAC nomenclature. Br (A) 3-bromo-2-methylheptanone (B) 4-bromo-5-methylheptanone (C) 5-bromo-6-methyl-2-heptanone (D) 4-bromo-5-methylheptanal