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
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
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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