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- Formulate the reaction. Explain the stereochemistry of the products based on the mechanism of the reactions. H2SO4 Et!! Me 'Et ELOH HWhich is the major organic product of the reaction provided? O A O B O U A) ex Br B) Br₂, hv Br xx xx xx Br D) racemicConsider the following mechanism of reaction: CH3 CH, CH3 CH;C CH, + H-CI CH;CCH, + C: → CH;CCH, tert-butyl cation CI tert-butyl chloride In this reaction: The alkene and the carbocation intermediate are both nucleophilic HCl and CI" are both nucleophilic The alkene and HCI are both electrophilic The carbocation and CI" are both electrophilic The alkene and CI" are both nucleophilic AMeving to another question will save this response
- Zaitsev's Rule refers to: which alkene is favored in a product mixture O how resonance contributors stabilize cations/anions/radicals O the stereochemistry of reaction intermediates/transition states O the stability of carbocation intermediatesa Draw the structure of the intermediate (I) for the reaction below. Hg(O2CCH3)2 NaBH4 Product CH;OH H3C • Use the wedge/hash bond tools to indicate stereochemistry where it exists. If the reaction produces a racemic mixture, just drawv one stereoisomer.Give the Major product(s) and name the starting compound with stereochemistry: H2O H2O H2SO4 H,SO, HgSO,
- Provide the structure of the organic products(s), which result in the reaction below. (Hint: it's a substitution product; show stereochemistry joll| CI CH3 Br CH3CH₂OH CNWhat is (are) the major organic product(s) obtained from the following reaction? Br2 O (2R,3R)-dibromobutane meso-2,3-dibromobutane O (2S,3S)-dibromobutane O Racemic mixtureIdentify the following pericyclic reaction; explain the course and stereochemistry of the reaction.
- Which statement best describes the stereochemistry of the product?Identify the carbocation intermediates first formed in the following reaction. Will rearrangements possibly occur? What major product is formed? $ HCIThe following nucleophilic substitution occurs with rearrangement. Suggest a mecha- nism for formation of the observed product. If the starting material has the S configura- tion, what is the configuration of the stereocenter in the product? NaOH OH H,0