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Topic: Acid Base Reaction Theory  (Read 3947 times)

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Offline w451208

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Acid Base Reaction Theory
« on: October 18, 2010, 09:50:06 PM »



Could someone explain why these answers are correct?

Offline MissPhosgene

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Re: Acid Base Reaction Theory
« Reply #1 on: October 18, 2010, 10:01:44 PM »
http://evans.harvard.edu/pdf/evans_pKa_table.pdf

87: B is the answer because the pKa of a terminal alkyne is much higher than the pKw. Therefore, the alkynyl anion will deprotonate water.

88: same as 87 except that methanol would be the favored deprotonated species at equilibrium.

pKa acetylene: 24. pKw= 15.7. pKa methanol = 15.5

Compare pKa values. You want the products to contain the conjugate base of the strongest acid in the reaction.
Stereograms of the 32 crystallographic point groups: little bike wheels of cold, hard, pure rationality.

Offline w451208

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Re: Acid Base Reaction Theory
« Reply #2 on: October 18, 2010, 10:18:20 PM »
Thanks for your reply could you explain it a little more in detail. The book I use for class sucks. What exactly am I looking for if this were on a test with out having any chart to help me?

Offline MissPhosgene

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Re: Acid Base Reaction Theory
« Reply #3 on: October 18, 2010, 10:52:55 PM »
I think that you may want to know approximate pKa values. Not memorize the list, but know about the groups you have used in class.

You might be able to organize by class of compound:

alcohol= around 15
sp carbon= around 25
sp2 carbon= about 50
sp3 carbon= greater than 50
carboxylic acid: usually 4 or less.
etc

Combining knowledge of relative base and acid strength is important to getting these questions right. You will always have the conjugate base of the strongest acid on the product side if the reaction is favorable. In other words, the molecule with the lowest pKa will exist in deprotonated form.

Stronger acid (lower pKa): most stable conjugate base. Strong acids have their dissociation ability because the conjugate base can stabilize a negative charge and therefore have decreased reactivity compared to the conjugate base of a weaker acid.

Weaker acid (higher pKa): not so good at stabilizing negative charges. Therefore, the conjugate base is more reactive and can do deprotonations more effectively than the conjugate base of a stronger acid.

When you have problems like this, look at the protonated species on each side of the reaction equation. If there is a stronger acid on the reactant side, the reaction goes as written. If the stronger acid exists on the product side, the reaction is disfavored and will not go as written.

I hope this helps.

Stereograms of the 32 crystallographic point groups: little bike wheels of cold, hard, pure rationality.

Offline Jorriss

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Re: Acid Base Reaction Theory
« Reply #4 on: October 19, 2010, 01:19:40 AM »
Just a note, look carefully at each question.

You should be able to easily narrow down 87 to two options.

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