1. Using a reaction coordina1e diagram, rationalize the fact that a teniary alkyl halide undergoes Ss 1 reaction while a primary alkyl halide will never do an Ss 1 reaction. /"-s, Hp* /"-OH .,..j]l...

Please, solve 11 problems of Organic Chemistry I with neat hand writing or through word file so I can understand them well.


1. Using a reaction coordina1e diagram, rationalize the fact that a teniary alkyl halide undergoes Ss 1 reaction while a primary alkyl halide will never do an Ss 1 reaction. /"-s, Hp* /"-OH .,..j]l not happen :;,l., H,O -)_OH &s< 3.="" predict="" the="" product="" of="" the="" following="" reactions.="" ho~="" nac="" n="" ~="" i="" nasl-1="" v="" ---="" d="" d="" d="" 4.="" fill="" in="" the="" missing="" rcagent(s)="" or="" product(s).="" ph,q="" nao="" et,="" etoh="" cl="" h,o=""> an elimination reaction under the given conditions. \Vha1 type of elimination would normall}' occur under these conditions? Why will it not occur for this particular compound? Explain in detail. NaOEt.EtOH 9. For which of the following reactions would elimination be the more favored pathway? Explain your answer. · 'l - Ph __ N_'•N~',~-.,..,. r, ..._...,,.. DMSO ~Ph NaN, OMSO a IO. Synthesize the following molecules starting with three carbons or fewer. 1~ 1 11. Name the following compound according to the IUPAC system of nomenclarurc. 12. Carlx:nes arc reactive intermediates that we have not discussed in class. The Lewis structure for dichlorocarlx:ne is shown lx:low. How would you expect dichlorocarbcne to react with cyclohexcne? Predict a product and a mechanism that justifies its formation. 0 :y1: : c..._c·1 :
Nov 17, 2021
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