Lab 3: Synthesis of Esters Flashcards

1
Q

What mechanism does this proceed under?

A
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2
Q

What are the limitations of this experiment? What can you do to remedy them?

A

Equillibrium favors both the carboxylic acid and the ester evenly. To remedy: push equilibrium

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3
Q

Why would waiting longer not result in a larger yield of ester?

A

Because everything will already be reacted

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4
Q

How are acetic acid and water removed from the product picture via extractions?

A

Sulfuric acid (removed by water), acetic acid (removed by bicarbonate), water (removed by brine)

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5
Q

What are the reagents in this reaction? What is their safety stuff?

A

Sulfuric acid: Highly corrosive, releases lots of heat with water, severe damage if ingested, reactive towards lots of other stuff

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6
Q

How can NMR be used to determine your starting product?

A

Look at the shifts of adjacent Hs and the alcohol H

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7
Q

How can you force the equilibrium?

A

Two ways the reaction can be pushed towards the ester product is by removing the water produced during the reaction from the system and by adding excess amount of acid.

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8
Q

why is it necessary to rinse the alcohol in graduated cylinder with acetic acid?

A

The alcohol is the limiting reagent, so it is important that all of the alcohol actually makes it into the reaction flask.

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9
Q

What is the purpose of the boiling stone?

A

A boiling stone is used to help the liquid boil more smoothly, reduce splashing, and not become overheated too quickly.

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10
Q

X acid of IR

A

wavenumber (cm^-1)

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11
Q

Y axis of IR

A

Absorbance (100%=no light absorbed)

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12
Q

During extractions ester is in what layer?

A

Organic layer, not charged

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