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- Instructions. Briefly describe the following given reactions. 2. The conversion of benzaldehyde into benzophenone. HNO, SOCL, (Oxidation) Benzaldehyde (Friedel-Craft acylation) Anhyd. AICI, Benzophenone AN SWERS: DeskClick the "draw structure" button to launch the drawing utility. Draw the product formed wvhen the following compound is treated with two equivalents of CH3CH,CH,CH,MgBr followed by H,O. of OCH, draw structure ...2. Provide synthetic route for the following transformation mia CI
- 3. Provide a synthetic route to each of the following compounds. b. OH H NH₂ from and anything elsePropose a curved arrow mechanism to account for the following transformation. or N. 'HKCN, EtOH Reflux N. OHc) Rank the following compounds in order of increasing reactivity toward nucleophiles. Explain your reasoning briefly with reference to structural features. or wy CI A
- Provide mechanism (arrow pushing) for this Friedel Crafts alkylation, include electrophile and resonance structures Benzene Cat. H2SO4Othesis. teps neceossary to synthesize this compound by yl halide; after that you can add any organic or Dound. →1-hexanol )Consider the following compounds: B = HOCH2CH2CH2CH3 CH3 HC C = CH3CH2CH2OCH2CH2CH3 D = a) Which one(s) could be reduced with NaBH4? b) Which one(s) would give a positive Tollens silver mirror test? c) Which one(s) could be oxidized with CrO3? d) Which one(s) would react with 1 or 2 equivalents CH3M9B to make a npound butyl ethyl ether larger alcohol?C. Draw the structure for the product formed in each of step of the following synthetic sequences. 1. C NH₂ SOCI₂ or P₂O5 or POCI3 (dehydration) 1.CH3MgBr 2.H3O+ 1. NaOH, 12 2. H3O+ + yellow precipitate
- 2, Solvolysis is referring to substitution reastions here The Solnenk i's study in ves kigaked the meehansm of solwolysis of varlous benzyl Chlorider. also the nucleophile, A diffenent, Adiffenent Hzo > SNI compound A > SN2 The Study Concluded that Compound A proceeded vin sNI pathway while eemp onnd B procelded Va sNa pathway a sUggest an explanation as to that is the case. 2 support your the SNI reaction of componnd A nexplanatiion bey gin'ng the full melhanism ofPlese don't provide handwritten solition..8. Outline a reasonable synthesis for the following molecule given the indicated starting material. You may use any reagent/s necessary. You must show all intermediate products. a. OH O M741-Group09. Ormord