Part 2.2 Having identified the expected products for elimination of cis-1 we can now perform a similar analysis for trans-1. Q8) groups axial or equatorial position clearly shown. Accurately draw the two chair conformations for trans-1 with the alcohol and methyl ОН CH3 trans-1 conformer A conformer B Q9) Which conformer of trans-1 is more stable and why? Q10) appropriate illustration indicate whether the more stable conformer of trans-1 can undergo E2 By considering the stereochemical requirements for E2-elimination, and using an elimination .

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Part 2.2 Having identified the expected products for elimination of cis-1 we can now perform a similar
analysis for trans-1.
Q8)
groups axial or equatorial position clearly shown.
Accurately draw the two chair conformations for trans-1 with the alcohol and methyl
ОН
„CH3
trans-1
conformer A
conformer B
Q9)
Which conformer of trans-1 is more stable and why?'
Q10)
appropriate illustration indicate whether the more stable conformer of trans-1 can undergo E2
elimination ·
By considering the stereochemical requirements for E2-elimination, and using an
Transcribed Image Text:Part 2.2 Having identified the expected products for elimination of cis-1 we can now perform a similar analysis for trans-1. Q8) groups axial or equatorial position clearly shown. Accurately draw the two chair conformations for trans-1 with the alcohol and methyl ОН „CH3 trans-1 conformer A conformer B Q9) Which conformer of trans-1 is more stable and why?' Q10) appropriate illustration indicate whether the more stable conformer of trans-1 can undergo E2 elimination · By considering the stereochemical requirements for E2-elimination, and using an
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