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Hi there! I would appreciate your help on 3 OC questions from the DAT Destroyer 2015 edition.
1. #13: Why would the para isomer crystallize out of solution and the ortho not? Also, how would column chromatography help separate the two...the way I see it, they both have dipole moments and are polar.
2. #20- The problem says that in steam distillation, the mixture distills at a temperature below the BP of the lower boiling component. I thought that distillation happens when the lower boiling component is vaporized while the higher boiling component isn't- so shouldn't it be above the BP of the lower boiling component?
3) #31- Why is choice B considered to have electron withdrawing groups? I thought NH2 was an activator/electron donor and that it was the most basic compound to the ones provided.
Thank you for your help in advance!
1. #13: Why would the para isomer crystallize out of solution and the ortho not? Also, how would column chromatography help separate the two...the way I see it, they both have dipole moments and are polar.
2. #20- The problem says that in steam distillation, the mixture distills at a temperature below the BP of the lower boiling component. I thought that distillation happens when the lower boiling component is vaporized while the higher boiling component isn't- so shouldn't it be above the BP of the lower boiling component?
3) #31- Why is choice B considered to have electron withdrawing groups? I thought NH2 was an activator/electron donor and that it was the most basic compound to the ones provided.
Thank you for your help in advance!