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- Draw a structure for the product of nucleophilic substitution obtained on solvolysis of tert-butyl bromide in methanol, and arrange the correct mechanism for its formation. Be sure to answer all parts.13.45 What reagents are needed to convert cyclopentene to (a) bromocyclopentane; (b) trans-1,2-dibromocyclopentane; (c) 3- bromocyclopentene?1. Draw the structure of all reactants and product for the following reactions. (a) 2-methyl-1-iodocyclopentane + NaOCH3 ------>A (b) A + (1) Hg(OAc)2, H2O/(2) NaBH4 ------>
- Draw the expected major product when 1-octene reacts with Cl2 in aqueous solution (with H2O as the solvent).6) 25pts. Draw the structure of the major alkene product (or products) formed by treatment of each of the following haloalkanes with sodium ethoxide in ethanol. Assume the mechanism is E2 elimination. t-BuO K t-BUOH Br CH3 Eto Na F ETOH CH2CH3 CI H- Eto Na -CH2CH3 ELOH H- ČH3 Br Eto Na ELOH CH3 CI, H Eto Na CH2CH3 H3C H D ELOHDraw the structure of the major product of benzene + CH3CH2CH2Cl in AlCl3
- Draw all possible products formed when 2-methylbut-2-ene undergoes addition with HCl. Label them as being either the major or the minor product.Hw.114.Chemistry 60. Give the principal product(s) expected, if any, when trans-1,3-pentadiene reacts under the following conditions. Assume one equivalent of each reagent reacts unless noted otherwise. (a) H2O, H3O+ (b) Na+EtO- in EtOH (c) Maleic anhydride heat