Saturday, April 30, 2005

Lecture 015: Wheel of Orgo

We played "Wheel of Orgo" today, which is basically a review session based on a game format. Students who participated drew a single step for a synthesis on the tablet PC during their turn. One point for the step, one point for correcting a mistake in a step and 3 points for completing the synthesis. Congrats to today's winner Sujeet!

If you are taking the class online and would like to participate in a future Wheel of Orgo session email me so that I can plan future sessions.

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Thursday, April 28, 2005

Lecture 014: review for test 1

In this review session I tried to show how to practice the class material by coming up with multiple syntheses for the same target molecules. If you are not coming to class make sure to email me your questions.

At the start of the session I explained how to access older items in the blog using the post links. You can also just scroll down.

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Tuesday, April 26, 2005

checklist for test

I noticed that the covered material section in the syllabus was outdated so I just updated it to reflect what we actually covered in class in the proper order.

Lecture 013: enols part 2

We looked at the second part of the enol section. This included Claisen condensation between esters and the crossed Claisen condensation between 2 different esters or between ketones and esters. Other synthetic strategies included the malonate ester and acetoacetic acid syntheses. Finally, Michael addition was covered.

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Saturday, April 23, 2005

Lecture 012: Enols part 1

We looked at enol reactions including alpha substitution with halogens, the haloform reaction aldol condensations. Variations on the aldol condensation such as crossed and intramolecular were covered. The detailed mechanism of acid and base catalyzed aldol was presented.

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Thursday, April 21, 2005

Lecture 011: Carboxylic Acids and their derivatives

We looked at carboxylic acids and their derivatives in terms of nomenclature, synthesis and reactions.

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Tuesday, April 19, 2005

Lecture 010: solution to problems 5 - 7

Problems 5, 6 and 7 covered amines.

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Saturday, April 16, 2005

Lecture 009: Solutions to probs 3 - 4

Problems 3 and 4 covered aldehydes and ketones.

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Thursday, April 14, 2005

Question about imines

Q:
Today in lecture, you were showing us how an amine can react to form
an imine by reacting with a carbonyl compound and acid. You also said
that the imine can be hydrolyzed back to the amine and carbonyl
compound by adding aqueous acid. One of the products of the reaction
you showed us today was water, so does that water and the acid thats
already present hydrolyze the imine back to the amine and ketone to
some extent to form an equilibrium? Also, is there a way to minimize
the hydrolysis back to the amine and ketone and keep the imine?

A:
Yes, it is an equilibrium. If you remove water you can drive the formation of the imine. Water can be removed using molecular sieves or distillation, depending on the reactants.

Lecture 008: Amines

We looked at amines - nomenclature, reactions and preparation.

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Tuesday, April 12, 2005

Lecture 007: Ketone Reactions

We looked at ketone and aldehyde reactions.

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Saturday, April 09, 2005

Lecture 006: Problem 002 and Ketone Preparation

Here are the solutions to synthesis problem 002 on aromatics. We also covered the rest of the preparation methods for aldehydes and ketones.

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Thursday, April 07, 2005

Lecture 005: Solutions to Problem 001

Here are the solutions to problem 001 on aromatics.

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Tuesday, April 05, 2005

Lecture 004: Benzyne, Aldehydes and Ketones - preparation

We finished up aromatics looking at the benzyne mechanism, side-chain oxidation with permanganate and a review of a few reactions like free radical halogenation and elimination at the side chain. Reviewed the nomenclature of ketones and aldehydes and listed methods of their preparation.

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Monday, April 04, 2005

Problem set

Here are the first questions of the Problem Set.

1) Predict the products from the reaction of toluene, nitrobenzene and m-chlorotoluene with:
a) 1-chloropropane/AlCl3
b) KMnO4 (hot, concentrated)
c) HNO3/H2SO4
d) HNO3/I2
e) AlI3/I2
f) t-butanol/BF3
g) SO3/H2SO4
h) Br2/light
i) PhCOCl/AlCl3
j) NaNH2
k) Br2/FeBr3
l) NaOH, 350C

2) Propose a synthesis of the following from benzene:
a) n-propylbenzene
b) m-chloronitrobenzene
c) p-iodoanisole
d) o-methylaniline
e) 1-bromo-1-phenylethane
f) methylcyclohexane

3) Predict the products from the reaction of benzaldehyde with:
a) Na2Cr2O7/H2SO4
b) KMnO4
c) PhMgBr then H3O+
d) CH3CH=PPh3
e) Ethylene glycol, H2SO4
f) HCN then H3O+,heat
g) NH2OH, H+
h) Acetone dimethyl ketal
i) NaBH4
j) NaBH3CN
k) NaBH3CN/isopropyl amine

4) Propose the synthesis of:
a) methyl ethyl ketone from 1,3-dithiane
b) benzaldehyde from toluene
c) acetophenone from ethynylbenzene
d) benzophenone from cyanobenzene
e) acetone from acetic acid
f) propionaldehyde from CH3CH2COCl
g) 2-hydroxybutanoic acid from propanoic acid

5) Predict the products from the reaction of 2-aminobutane with
a) methyl bromide (excess)
b) methyl bromide (excess) then Ag2O then heat
c) diethylamine/NaBH3CN
d) bromobenzene
e) benzoyl chloride then LiAlH4

6) Predict the products from the reaction of aniline with
a) NaNO2/HCl then H3O+
b) NaNO2/HCl then CuBr
c) NaNO2/HCl then CuCl
d) NaNO2/HCl then CuF
e) NaNO2/HCl then HBF4
f) NaNO2/HCl then H3PO2
g) Br2/FeBr3

7) Propose a synthesis of:
a) diethylmethylamine from ethylamine
b) phenylisopropylamine from benzene and acetone
c) meta-bromofluorobenzene from benzene
d) benzylamine from toluene
e) methylamine from CH3CONH2
f) 1-amino-2-phenylethane from benzylbromide
g) p-nitroaniline from aniline

8) Predict the products from the reaction of propanoic acid with:
a) LiAlH4
b) NaOH
c) acetyl chloride
d) CH3MgBr

9) Propose a synthesis of:
a) propanoic acid from 1-propanol
b) propanoic acid from ethanol
c) acetic acid from 2-pentyne
d) CH3NHCH2CH3 from acetic acid
e) CH3COOCH2CH3 from acetic acid
f) Acetic anhydride from ethanol
g) Acetophenone from an organocuprate

10) Draw the mechanisms for the formation of an amide from ammonia and CH3COOCH2CH3

11) Predict the products from the reaction of:
a) cyclohexanone with Br2(one equivalent)/CH3COOH
b) acetophenone with I2(excess)/NaOH
c) propanal with NaOH
d) 2-butanone with benzaldehyde(excess), H2SO4/heat
e) propanal with formaldehyde(excess), H2SO4/heat
f) 2,7-octanedione with NaOH/heat
g) 2,6-octanedione with H2SO4/heat
h) 2,5-octanedione with NaOH/heat
i) 2,4-octanedione with NaOH/heat
j) CH3CO2Et with NaOH
k) CH3CO2Et with NaOEt
l) CH3CO2Et with benzaldehyde(excess), NaOEt
m) CH3CO2Et with oxalic acid (HO2CCO2H) (excess), NaOEt
n) Diethyl malonate with 1) NaOEt 2) benzyl bromide 3) H3O+
o) Ethyl acetoacetate with 1) NaOEt 2) n-propyl bromide 3) H3O+
p) Cyclohexanone with 1) NaOH/methyl vinyl ketone/heat

12) Using an enolate reaction propose a synthesis of:
a) bromoacetone
b) methyl vinyl ketone
c) PhCH2CH2COCH3
d) PhCH2CH2COOH
e) PhCOCH2COOEt
f) PhCOCH2COPh
g) CH3CH(OH)CH2CHO
h) CHCl3

Saturday, April 02, 2005

Lecture 003: Ortho Meta Para

We first covered a few more electrophilic aromatic substitution reactions such as nitration, sulfonation and Friedel-Crafts acylation. The advantage of using acylation followed by a Clemmensen reduction over Friedel-Crafts acylation was discussed. Hydrogenation of the aromatic ring was briefly looked at. Most of the lecture involved accounting for ortho/para and meta directing groups, as well as activating and deactivating effects.

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