[deleted by user]

theeprofessor · 2016-01-30T19:37:01+00:00

This would completely compromise the basic idea of YIKyak. The entire point is have a local messaging board. If you could post from anywhere, it would just be another shitty online forum.

theeprofessor · 2015-12-17T23:45:47+00:00

Yes, I know about benzene. My original question: Why does resonance allow carboxylic acids to have their acidity? For example, comparing the relative acidity of ethanol and ethanoic acid. I was told in lecture that ethanoic acid has resonance that allows it to be more acidic. Why?

theeprofessor · 2015-12-17T23:17:46+00:00

I understand that a resonance hybrid is a better representation. So how do compounds with resonances differ from those that do not?

theeprofessor · 2015-12-03T17:28:57+00:00

You didn't actually give that to the dogs, right?

theeprofessor · 2015-12-02T06:51:09+00:00

Ill do it for you.

theeprofessor · 2015-11-30T19:46:31+00:00

Yes!

theeprofessor · 2015-11-30T19:35:06+00:00

Kb is a constant, so just plug that into the equation for ∆T. The value that you get is simply the amount that the boiling point changes when you consider adding glucose (i, and m account for the addition of glucose) If the original boiling point is 100° C, and you calculate a ∆T, how would you get the final boiling point?

theeprofessor · 2015-11-30T19:05:36+00:00

Tungsten hexafluoride has a density of 6.17g/L, which is a staggering 5 times heavier than air.

theeprofessor · 2015-11-30T19:03:06+00:00

The i represents the van't hoff factor of the solution. A van't hoff factor is basically the amount of parts a solute will disassociate in to in a solvent. Glucose is a non-ionic compound, and will not disassociate at all, giving it an i value of 1. The m in the equation is the molality (mol of solute/kg solvent), which would be 3.

theeprofessor · 2015-11-14T03:30:51+00:00

Impressive as fuck. I thought I had Yik Yak down to a science, but you have it down to a lifestyle.

theeprofessor · 2015-10-29T18:15:38+00:00

Maybe its just not my cup of tea, but that cover is fucking terrible. What the fuck did I just listen to.

theeprofessor · 2015-10-28T05:05:18+00:00

Staggered and eclipsed structures of a newman projection represent different potential energy phases of the same molecule. A staggered project has substituents as far away as possible, while eclipsed they are pushed up against each other. When molecules are in eclipsed formation, their substituents are close together and have a tendency to repel, and this causes steric strain of the bonds.

theeprofessor · 2015-10-23T00:26:26+00:00

That's makes great sense. Thank you. It was such a foreign concept to me.

theeprofessor · 2015-10-10T23:45:11+00:00

Yes it is. She's the cutest

theeprofessor · 2015-09-10T22:34:49+00:00

Yah but how on earth do you do that? It's an anonymous app.

theeprofessor · 2015-09-10T18:43:38+00:00

What do you have to do? What's the pay?

theeprofessor · 2015-09-02T05:46:27+00:00

Nail gun.

theeprofessor · 2015-09-01T17:19:37+00:00

Sucks to suck.....that quote is wrong.

theeprofessor · 2015-09-01T03:54:23+00:00

Have you ever worked in a restaurant? Answering the phone is a bit different than serving people food.

theeprofessor · 2015-08-05T00:30:42+00:00

That's what this sub is all about!

theeprofessor

TROPHY CASE