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- This reagent produces alcohols from alkenes and adds primarily in a Markovnikov orientation 1) Hg(OAc)2, H2O; 2) NaBH4 1) O3; 2) (CH3)2S PCC KMnO4 Na2Cr2O7/H2SO4Draw all of the substitution and elimination products formed from thegiven alkyl halide with each reagent: (a) CH3OH; (b) KOH. Indicate thestereochemistry around the stereogenic centers present in the products,as well as the mechanism by which each product is formed.(a) 2-methyl-2-pentanol Draw the structure of the alkene that was used to prepare the alcohol in highest yield. ? ChemDoodle Which process does this employ? 1. Hg(OAc)2, H₂O; 2. NaBH4 1. BH3; 2. H₂O2, NaOH OsO4, H₂O2 √ [F
- None5. Conjugate vs Direct Addition Draw the major organic product formed for each reaction. (a) (b) H NaSCH3 HSCH3 ная H3C. LiAlH4 then H₂O(b) 1,2-hexanediol Draw the structure of the alkene that was used to prepare the alcohol in highest yield. / / ? ChemDoodleⓇ Which process does this employ? 1. Hg(OAc)2, H₂O; 2. NaBH4 1. BH3; 2. H₂O2, NaOH 0804, H₂O2 Sn [F
- Which of the following compounds have an stereogenic center? H;C CH: H. H. CH CH H- CH(CH,) ČH;CH;CH,For A-F please clasify what defintion it is in the next photoFor each IUPAC name, draw the complete structure. (a) (25,3R.4R)-2,3-diamino-4-hydroxycyclopentanone; (b) (2R.3R)-2-butyl-3-hydroxypentanedial: (c) (4S,5R)-4.5-diaminoheptane-2,3,6-trione: (d) (3E,5R,6Z)-5-hydroxy-7-methoxyocta-3,6-dien-2-one