Exam 1 Flashcards

1
Q

Definition of Polymers

A

Large macromolecules which are made of many repeating units of smaller molecules.

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2
Q

Types of polymers

A
  • Addition polymers
  • Condensation polymers
  • Polyamides
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3
Q

Definition of Addition polymers

A

monomers’ double bonds are broken and the molecules form a long chain

Ex- polyethylene, polyvinyl chloride, polystyrene.

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4
Q

Def of Condensation polymers

A

Bifunctional monomers react to form a long-chain polymeric molecule

Ex- Nylons, polyesters, polysaccharides.

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5
Q

def of Polyamides

A

formed when compounds with a COOH functional group react with NH2 group.

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6
Q

What does the number after nylon mean?

A

The number of carbon atoms present in each of the original reactants.

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7
Q

What technique was used to prepare Nylon in the lab?

A

Interfacial Polymerization (reaction occurs at the interface of two solutions)

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8
Q

Why was sebacoyl chloride used instead of carboxylic acid in the nylon reaction?

A

Acid chlorides are much more reactive than acids are

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9
Q

Why is NaOH used in the Nylon Reaction?

A

It is used to neutralize the HCl byproduct of the reaction

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10
Q

Why are plasticizers added to polymers?

A

They help to improve the flexibility and extensibility of the polymer

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11
Q

Chemiluminescence Definition

A

The emission of light as the result of a chemical reaction

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12
Q

What is the name of the chemical responsible for firefly light?

A

Luciferase

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13
Q

What is the chemical responsible for producing light in a glow stick?

A

Luminol and Oxalate reactions

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14
Q

Practical uses of compounds with chemiluminescent properties

A
  • Forensic science
  • Spectroscopy
  • Medical diagnosis
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15
Q

Diene Definition

A

unsaturated hydrocarbon containing two double bonds. Must be conjugated and in s-cis- conformation.

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16
Q

Dienophile Def

A

An alkene or Alkyne that readily reacts with a diene.

17
Q

Adduct Def

A

The product of the diels alder reaction incorporating the reactants

18
Q

What is the thermometer reading during the collection of cyclopentadiene?

19
Q

Why is cyclopentadiene prepared right before using it?

A

If stored at room temperature, it is completely converted into the dimer.

20
Q

How was cyclopentadiene added to the solution of Maleic anhydride?

A

It was added using a dropper while the anhydride was in an ice bath

21
Q

Why was Cyclopentadiene added slowly to maleic anhydride?

A

The reaction is exothermic and overheating with splashing will occur if the cyclopentadienyl is added too fast.

22
Q

Why was a mixture of solvents used in the DA rxn?

A

To maintain thermal equilibrium so the adduct will form

23
Q

Why is the nitration of methyl benzoate performed at a low temp?

A

Temp must be kept below 15 C to prevent the formation of byproducts.

24
Q

How was the filtrate neutralized?

A

The filtrate is poured into 30 ml of water and 8g of Sodium carbonate is added

25
The main product of nitration of methyl Benzoate
The reaction is regioselective, Methyl 3-nitrobenzoate
26
What are some possible side products of Nitration if the temp is not kept low?
The methyl 3,5 Dinitrobenzoate product
27
Why is the yield of the nitration reaction low?
multiple vacuum filtrations