developing critical thinking problems for organic chemistry

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Developing Critical Thinking Problems for Organic Chemistry. Ray A. Gross, Jr. Prince George’s Community College. January 10, 2007. Thoughts About Students. They do not spend enough time working problems. They need to be taught (learn) how to reason. - PowerPoint PPT Presentation

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1

Developing Critical Thinking Problems for Organic

Chemistry

Ray A. Gross, Jr.

Prince George’s Community College

2

January 10, 2007

3

Thoughts About Students

• They do not spend enough time working problems.

• They need to be taught (learn) how to reason.

• One way to force them to reason is to give them problems they have not seen before.

4

Nature of the Problems

• Focused on developing reasoning skills• Solvable by applying course content • The amount of content is limited

5

Kinds of Problems Available

• Spectroscopy

• Synthesis

• Degradation*

6

Concept of Degradation

A compound of unknown structure is broken down into smaller pieces, which can be reassembled in a logical way to determine the structure.

7

Example of Ozonolysis

+CH3CH2CCH3

O

CH3CH2CH

O

Xunknownhydrocarbon

(1) O3

(2) Zn/H+

remove oxygen

CH3CH2CCH3+ CH3CH2CH

anathons

CH3CH2CCH3

HCCH2CH3

analyte

8

O3

(R)

C7H14C4H8O C3H6Oketone aldehyde

+

+

C4H8C3H6

anathons

analyte

Cleavage of a double bond yields two carbonyl compounds,aldehydes or ketones.

9

Some Aldehydes may be identified by their molecular formulas.

C

O

H HCH2O = C

H H

molecularformula

structuralformula

anathon

10

=

molecularformula

structuralformula

anathon

C2H4OC

O

CH3 HC

CH3 H

Some Aldehydes may be identified by their molecular formulas.

11

Consider the following reaction.

C3H6

O3

(R)CH2O + C2H4O

Given only molecular formulas.

12

Anathons are like building blocks.

C3H6

O3

(R)CH2O + C2H4O

CH H

O+

CH3CH

O

CH H CH3CH

+

CH

HC

H

CH3

propene

13

+CH3CH2CCH3

O

CH3CH2CH

O

(1) O3

(2) Ag2O

(1) O3

(2) Zn/H+

CH3CH2CCH3

O

CH3CH2COH

O

+

ketone

ketone

aldehyde

acidCH3CH2C CHCH2CH3

CH3

Ketones remain ketonesAldehydes are oxidized to acids

14

(1) O3

(2) Ag2O

(1) O3

(2) Zn/H+

+C7H14

C4H8O C3H6O2

C4H8O C3H6O+

Same reactions using molecular formulas.

15

Identify aldehydes and ketones.

(1) O3

(2) Ag2O

(1) O3

(2) Zn/H+

+C7H14

C4H8O C3H6O2

C4H8O C3H6O+

no change

ketone

plus 1 O

aldehyde

Result: A four-carbon ketone and a three-carbon aldehyde.

16

Place C atoms in logical locations to find anathons.

Connection of anathons reveals the unknown’s structure.

C7H14C4H8O C3H6O

ketone aldehyde

anathons

17

Concept

• Degradation of an unknown leads to products.

• The structure of each degradation product can be determined directly or indirectly from the two kinds of ozonolysis.

• The products can then be converted into anathons, which are connected in a logical way to produce the starting compound.

18

Producing Solvable Problems

• Find structures that are deducible from the two kinds of ozonolysis reactions.

• Convert them into anathons.• Join anathons to make unknowns.

19

Structures from Molecular Formulas

CH2O CO2 H C H

O

C2H4O C2H4O2 CH3CH

O

C3H4O C3H4OO

(R) (O) R product

20

Remove Oxygen to form Anathons

CH2O CO2 H C H

O

C2H4O C2H4O2 CH3CH

O

C3H4O C3H4OO

(R) (O) R product Anathon

H C H

CH3CH

21

Join Anathons to Create Unknowns

Anathon

H C H

CH3CH

H2C CHCH3

H2C

CH3CH

Unknown

The process ensures solvable structures are produced.

22

Internal Anathons

• When a molecule is cleaved in two places, the middle compound produces an internal anathon.

23

Example of an Internal Anathon

H2C CHCH2CH=CHCH3

O3 (O)

O3 (R) CH2O + C3H4O2 + C2H4O

CO2 + C3H4O4 + C2H4O2

HCH HCCH2CH CH3CH

terminal anathon

terminal anathon

internal anathon

24

Carbon-Carbon Triple Bonds

• Ozonolysis by either workup gives two carboxylic acids.

25

Cleavage of a Triple Bond

CH3C CCH2CH3

CH3CO2H + CH3CH2CO2H

CH3CO2H + CH3CH2CO2HO3 (O)

O3 (R)C5H8

A triple bond in the analyte leads to two new hydrogen atoms and four new oxygen atoms.

26

O3 (R)C5H8 C2H4O2 C3H6O2+

2 new H atoms = triple bond two caboxylic acids

CH3C CCH2CH3

Anathons from triple bonds have three bonding sites, andthose from double bonds have two.

27

Anathons Readily Determined by their Ozonolysis Products

• 11 Terminal Anathons

• 11 Interior Anathons

• 3 Either Terminal or Interior

306 unique unknown hydrocarbons can be producedfrom the 22 anathons. All of them are solvable by the techniques shown.

28

Example of Terminal/Interior Anathon

terminal anathon

A secondterminal anathon is bonded here.

interior anathon

Threeterminal anathons are bonded as indicated.

29

Examples of the Unknowns

CH3CH2CH CHCH2CH C(CH3)2

CH3CH2CH C CCH3

CH2CH3

CHC CCH2CH3

30

Problems Created that:

• Students have never seen before• Require a minimum amount of course content• Require students to apply logic and reasoning

(synthesis, analysis and evaluation)• Increase in complexity over the semester• Allow the instructor to give each student a

unique problem each week

31

The approach described might be of use in other chemistry courses or disciplines.

32

Problems of this type are available in the following references.

Chemical Educator 2006, 11, 372-377.

Journal of Chemical Education 2006, 83, 604-609.

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