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- Match each reagent to the product that it forms. Multiple reagents may form the same product. нох Reagent Reagents SOCI2, pyridine: C CISO2CH3, pyridine: E HCI: A PCI 3: A A) B) "It "ft "bl H₂O D) E) F) پہلے علی علیہHow would you prepare 3-phenyl-1-propanamine (C&H-CH₂CH₂CH₂NH₂) from C&H,CH₂CH₂CHO C HẠCH,CH,CHO Select the correct reagent for A. Ⓡ (CH,ANH, ơi (CH₂)NO > C HẠCH,CH,CH;NH, NaBH, CN CHÍNH, Ố NH₁ ?Ho M no- OH - -H HOH H- OH он + H₂N- o p Val, Braw arrow on Glycosylated val on on ENY on OH Be BH BH/B² ou pushing de protonations necessary. on the pathaway towards schiff base. and eventually Glycasylated Bual, NH سليب
- 1% 76 70- 60- 50 40- 30- 20 10- -of 4000 3505.81cm-1 acetophenone 3500 O 2-methylcyclohexanone benzoyl chloride benzyl acetate O butyrolactone O cyclopentanone methyl benzoate 3523.83cm-1 methyl propionate 2992 510m-1 3000 2817.24cm-1 2500 1769.54cm-1 cm-1 2000 N 930.88cm-1 1377.30pm-1 1500 1167.95cm-1 1000 1036.26cm-1 500Although codeine occurs in low concentration in the opium poppy, most of the codeine used in medicine is prepared from morphine (the principal component of opium) by the following reaction. Explain why selective methylation occurs at only one OH in morphine to give codeine. Codeine is a less potent and less addictive analgesic than morphine. но. CH,0. [1 кон H [2] CH3I H. CH3 H Ho morphine H. CH3 Ho codeinePrednisolone is a synthetic corticosteroid that is used as an anti-inflammatory agent. A НО НО HO B Which box contains carbonyl carbon? A Box A B Вох В both ....I ....I
- Match each reagent to the product that it forms. Multiple reagents may form the same product. HO Reagent Reagents SOCI2, pyridine: C CISO2CH3, pyridine: E HCI: A PCI 3: A A) B) "It eft ft D) E) F) "got soft soft MSO MsO CIGiven this retrosynthetic analysis, propose a synthesis for the antihistamine p-methyldiphenhydramine. Is p-methyldiphenhydramine chiral? If so, how many of the possible stereoisomers are formed in this synthesis? H NMe, НО Br p-Methyldiphenhydramine +arrow pushing mechanism to illustrate the formation of t-butyl bromide from t-butanol and draw in the necessary intermediates and products formed. 41. Draw an CH3 H3C- OH H FotH CH3 H. Conjugate Acid Conjugate Base CH3 H3C CH3 carbocation t-butyl bromide H,O