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CIIM-170 Assigtiment #LI Dar Apell 24, 20The. S00 ASE s amigineat huare 5-too di

ID: 518953 • Letter: C

Question






CIIM-170 Assigtiment #LI Dar Apell 24, 20The. S00 ASE s amigineat huare 5-too dificult) 1. Which base gives the highek yieki cE elimination produt upon reartmn with the alkyl alae a) CH,00k. b) Cr,ca,o- e) (CEIalycor d) CH3CH,S 2. Why are Protic gdwatx nachharail and Propanaa: eil anat ethstive at Trenet:ng SN1 reations? a) Ther tin up LEa utloophile in lydrs bonds b) Thry lxrwe:r Lleactivation etergy Soc Ss1ssechoran c) TMItalrikaz 1heoebucatios intermediate cal Therren't Protksuheirs prenote Bv2madanimy 3. How many, traasition states wrald he Preast in tim frMargy prifie repe watng thE follwing reactirn? Page 1 of 5

Explanation / Answer

1. Answer:- C

The percentage of elimination product depends on strength of base. Stronger the base more would be the percentage of elimination product. In given case option c is strongest base so it gives highest percentage of elimination product

2. Answer:- C

Polar protic solvent are more suited for SN1 reaction as they stabilise the carbocations formed.