Docsity
Docsity

Prepare for your exams
Prepare for your exams

Study with the several resources on Docsity


Earn points to download
Earn points to download

Earn points by helping other students or get them with a premium plan


Guidelines and tips
Guidelines and tips

Elementary Organic Chemistry In-Class Quiz 2 - September 2008, Quizzes of Organic Chemistry

A chemistry quiz focused on topics such as bronsted-lowry acids, pka values, and organic acids. It includes multiple-choice questions and an explanation for the acidity differences between the first and second ionization of carbonic acid.

Typology: Quizzes

Pre 2010

Uploaded on 08/04/2009

koofers-user-shb-1
koofers-user-shb-1 🇺🇸

1

(1)

10 documents

1 / 2

Toggle sidebar

This page cannot be seen from the preview

Don't miss anything!

bg1
NAME: September 26, 2008
OVER
Chemistry 231 – Elementary Organic Chemistry
In-Class Quiz -- #2
1. (6 pts. total; 3 pts. each) For each of the following questions, circle the BEST
answer.
a. Strongest Bronsted-Lowry acid
H
2
O H
2
S H
2
Se H
2
Te
b. Has the highest pK
a
CCl
3
CH
2
OH CBr
3
CH
2
OH CF
3
CH
2
OH CH
3
CH
2
OH
2. (4 pts) Carbonic acid, H
2
CO
3
, is a diprotic acid. That is, it can donate two protons.
In the space provided below, explain why the first acid dissociation of carbonic acid
(pK
a1
= 6.4) is greater than the second (pK
a2
= 10.3). You may find it helpful to use
a structural diagram.
Place your answer here
After the first ionization, there is a negative charge on the compound (this is
the bicarbonate anion). Removing a proton (H
+
) from a negatively charge ion
is more difficult due to Coulombic attraction. Hence, the pK
a
differences.
OC
O
OH
H
OC
O
O
H
OC
O
O
Bicarbonate
anion
pf2

Partial preview of the text

Download Elementary Organic Chemistry In-Class Quiz 2 - September 2008 and more Quizzes Organic Chemistry in PDF only on Docsity!

NAME: September 26, 2008

OVER 

Chemistry 231 – Elementary Organic Chemistry

In-Class Quiz --

  1. (6 pts. total; 3 pts. each) For each of the following questions, circle the BEST answer.

a. Strongest Bronsted-Lowry acid

H 2 O H 2 S H 2 Se H 2 Te

b. Has the highest p K a

CCl 3 CH 2 OH CBr 3 CH 2 OH CF 3 CH 2 OH CH 3 CH 2 OH

  1. (4 pts) Carbonic acid, H 2 CO 3 , is a diprotic acid. That is, it can donate two protons. In the space provided below, explain why the first acid dissociation of carbonic acid ( p K a1 = 6.4) is greater than the second ( p K a2 = 10.3). You may find it helpful to use a structural diagram.

Place your answer here

After the first ionization, there is a negative charge on the compound (this is the bicarbonate anion). Removing a proton (H+) from a negatively charge ion is more difficult due to Coulombic attraction. Hence, the p K a differences.

O

C

O

O

H

H

O

C

O

O

H

O

C

O

O

Bicarbonate anion

  1. (4 pts total, 2 pts each) Rank each of the following acids in order of increasing acidity (1 = strongest acid and 3 = weakest acid; 2 = the one in the middle)

a. CH 3 CO 2 H CH 3 CH 2 CH 3 CH 3 CH 2 OH

_____1____ _____3_____ _____2_____

b. CH 3 CH 2 CH 3 CH 3 CH=CH 2 CH 3 C≡CH

_____3_____ _____2_____ _____1_____

  1. (6 pts total) Proteins that catalyze chemical reactions in living systems are called enzymes. The basic building blocks of proteins are called amino acids and have the general structure pictured below where R is a substituent containing one of many organic functional groups. For clarification, some examples of amino acid R groups found in nature are pictured here.

R H 2 N H

CO 2 H

C

CH 3 H O H C

H H 3 C CH 3 CH 2 SH C

C O O

H H

H

An Amino Threonine Valine Cysteine Aspartic Acid Acid

a. Based on your knowledge of organic structure, identify which of the amino acid R groups pictured above corresponds to the following. Place your answer(s) in the space provided

Has a carbonyl group Aspartic Acid

Is neutral (not charged) at pH > 10 Threonine & Valine