When a photochromic spironyran is exposed to UV light, it forms an ionic form of isomer. In which solvent the onic form of the spiropyran will take a longer time to relax back to the original non-ionic isomer? . O cyclohexane toluene methyl alcohol xylene

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter4: Organic Compounds: Cycloalkanes And Their Stereochemistry
Section4.3: Stability Of Cycloalkanes: Ring Strain
Problem 8P: Each H↔H eclipsing interaction in ethane costs about 4.0 kJ/mol. How many such interactions are...
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When a photochromic spironvran is exposed to UV light, it forms an ionic form of
isomer. In which solvent the onic form of the spiropyran will take a longer time to
relax back to the original non-ionic isomer? .
O cyclohexane
toluene
methyl alcohol
O xylene
Transcribed Image Text:When a photochromic spironvran is exposed to UV light, it forms an ionic form of isomer. In which solvent the onic form of the spiropyran will take a longer time to relax back to the original non-ionic isomer? . O cyclohexane toluene methyl alcohol O xylene
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