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Identify the Lewis acid and Lewis base in each of the following reactions.
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GEN COMBO CHEMISTRY: ATOMS FIRST; ALEKS 360 2S ACCESS CARD CHEMISTRY:ATOMS FIRST
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- Please Don't used hand raitingarrow_forward7. For the following structure: ← Draw structure as is - NO BI H H Fisher projections (a) Assign R/S configuration at all chiral centers (show all work). Label the chiral centers with an asterisk (*). (b) Draw an enantiomer and diastereomer of the above structure and assign R/S configuration at all chiral centers (again, show all work). (c) On the basis of the R/S system, justify your designation of the structures as being enantiomeric or diastereomeric to the original structure.arrow_forwardDon't used Ai solutionarrow_forward
- 1. For the following reactions, predict the major product. Show stereochemistry where appropriate. неу b) 7 HBr XV ROOR H₂504 c) N/ H20 H+2 d) ~ Pt c) f. MCPBA -> сна сла (solvent) (1)BH 3-THE (3) Надрон B177 H20 9)arrow_forwardFor the following reactions, predict the major product. Show stereochemistry where approarrow_forwardHow is Talu home quer in Org. Chemistry propose a 3-butanal prepared from ketone? complete reaction for this, (to start from the guignand Meagent. ②what pocubble products could be produced from the reaction of : CA₂ CH₂ CH₂ dil H.504 A CH3 1 OBCH₂OH Naz Cr₂ 07 12504 NazCD 4 CH3CH2 07 AzS04 H3C H3C CH3-C - C - Atz но но + H, CH3 07 > ⑦Colts C614501 + (215) 504 кон 4arrow_forward
- Rank the following compounds most to least acidic: a) О OH 요애 OH .OH flow flow О F F F F OH F b) Ha EN-Ha CI Ha F F CI Haarrow_forwarda) b) Provide arrows to show the mechanisms and then predict the products of the following acid base reaction. Use pKas to determine which way the reaction will favor (Hint: the lower pka acid will want to dissociate) Дон OH Ha OH NH2 c) H H-O-Harrow_forwardMATERIALS. Differentiate between interstitial position and reticular position.arrow_forward
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