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ochem lab midterm

front 1

Distillation is the separation of multiple _____ components based on their different ______.

As the mixture is heated and the first component ____, its _____ form travels through the distillation set-up and ______ into a different container.

back 1

liquid, boiling points.

boils, vapor, condenses.

front 2

To insert a thermometer into an adapter, use _____ to prepare the thermometer. Then, hold the thermometer _____ the adapter and _____ the thermometer into the adapter.

back 2

mineral oil, close to, slowly turn

front 3

What are the concerns presented by overheating a distillation to a dry flask?

back 3

-> The empty glassware might heat quickly, igniting vapors from the distillation.

-> The remaining solid residue might contain explosive peroxides.

front 4

Before turning on the heat for a microscale distillation, what should you confirm about the set-up?

back 4

-> Secure connections at the joints

-> Presence of boiling chip in the sample

-> Existence of some opening in the set-up

front 5

Where should the tip of the thermometer be placed in a microscale distillation set-up?

back 5

At or slightly below the side arm of the distillation head

front 6

An azeotrope is a mixture that has _____ composition in the __________. Therefore, an azeotropic mixture _____ be separated by distillation.

back 6

the same, gas and liquid phases.

cannot

front 7

Suppose you are using distillation to separate cyclohexane and toulene. The boiling point of cyclohexane is ____ oC and the boiling point of toulene is ____ oC. Therefore, the liquid collected first should be ________.

back 7

81, 111, cyclohexane

front 8

Lab#2

Most desired compound from one layer to another ____

Often involves a reaction in one of the layers _____

Leaves desired compound in its starting layer _____

Movies impurities from one layer to another ______

Leaves impurities in their starting layer _____

back 8

1. Extraction

2. Extraction

3. Wash

4. Wash

5. Extraction

front 9

Suppose you are performing an extraction procedure with a carboxylic acid, like benzoic or toluic acid.

Which layer should contain the carboxylic acid in a two-layer mixture of water and an organic solvent, like diethyl ether?

back 9

The organic layer

front 10

You then add a base to form the corresponding carboxylate.

Which layer should contain the carboxylate in a two-layer mixture of water and organic solvent, like diethyl ether?

back 10

The aqueous layer

front 11

Suppose you are performing an acid/base extraction. After one of the steps, you have collected a NaOH extract containing phenolate.

Next, you add HCl to the layer. What are the products of the HCl solution?

back 11

The acid can donate a proton to the phenolate, forming phenol. Chloride ion is left after the acid loses a proton.

PhO- + HCl ----> PhOH + Cl-

front 12

What is the purpose of a drying agent in the work up of an organic reaction?

back 12

To absorb small amounts of water in an organic solution

front 13

When using acids and bases, note that these substances are ______. Make every effort to avoid contact with ___________. Be sure to wipe up any spills ________.

back 13

corrosive, the skin and lab surfaces, immediately

front 14

Aniline involves an amine, which is a _____ functional group. When an aqueous acid solution is added to an organic solution including aniline, the aniline appears in the ______ layer in its ______ form. Then, a base is added to ________ the aniline.

back 14

basic, aqueous, protonated, reconstitute

front 15

Identify the solution used for each described purpose.

Reconstitute aniline from aqueous layer ____

Reconstitute benzoic acid out out of the aqueous layer ______

Extract benzoic acid into the aqueous layer ____

Extract reconstituted 3-nitroaniline out of the aqueous layer ____

Extract aniline into the aqueous layer _____

back 15

1. 6 M NaOH

2. 6 M HCl

3. Dichloromethane

4. 5% NaOH solution

5. Dichloromethane

6. 5% HCl solution

front 16

What hazards are associated with napthalene?

back 16

-> Naphthalene is flammable

-> Naphthalene produces nauseating vapors

-> Naphthalene is toxic

front 17

Lab #3

Before adding a sample or solvent to a separatory funnel, what should you have in place?

back 17

-> A stopcock in the closed position

-> A funnel in the top of the separatory funnel

-> A flask under the separatory funnel

front 18

After mixing solutions in a separatory funnel, the stopper should be _____ and the liquid should be ________ and the layers allowed to separate.

When you get close to the interface between the layers, _______ the funnel and _______ until the first layer is collected. _______ to collect the second layer.

back 18

removed, drained through the stopcock

get eye level with, slow the draining

switch to a new flask

front 19

After an organic reaction involving an aqueous solution, the organic solution might be washed with a saturated sodium chloride aqueous solution, known as brine.

What is the purpose of the brine wash?

back 19

To reduce the amount of water in the organic solution.

front 20

What is the visual indicator that enough of a drying agent, such as anhydrous MgSO4 or CaCl2, has been added to properly dry an organic solution?

back 20

The drying agent will move freely like a powder around the solution.

front 21

After drying an organic solution, what methods can be used to remove the drying agent from the solution?

back 21

-> Decanting

-> Vacuum or gravity filtration

front 22

If crystal growth does not start on its own after the solution in the flask returns to room temperature, identify the best ways to promote this process.

back 22

-> Add a bit of solid as a seed crystal.

-> Scratch the bottom of the flask gently with a stirring rod.

front 23

What is the best course of action if solid material remains in the flask after the heating step of a recrystallization?

back 23

Filter the hot mixture.

front 24

In general, when hydrocarbons like oil are added to water, the two liquids ______ because hydrocarbons are _____ and water is ______.

back 24

do not mix, non-polar, polar.

front 25

Identify the characteristics of a good recrystallization solvent.

back 25

-> Dissolves a sample well at high temperatures

-> Does not dissolve a sample well at low temperatures

front 26

Identify the best support for a separatory funnel.

back 26

Iron ring clamped to a ring stand.

front 27

When using a separatory funnel, you should burp the funnel.

What does the therm burping mean?

back 27

Opening the stopcock when the flask is inverted during mixing.

front 28

When drying an organic solution, start by transferring the solution to ________ or a test tube, depending on the amount.

Then, add ________ of the drying agent and ______ to determine if you added enough drying agent.

Continue _______ until the solution is dry.

back 28

an Erlenmeyer flask

pea-sized amount, swirl the flask

adding small amounts

front 29

Identify the best drying agent or process for each described purpose.
Removal of small amounts of water from a polar solvent _______

Removal of visible pockets of water from an organic solvent ______

Storage of solvents or other materials in a desiccator _____

back 29

Anhydrous calcium chloride

Brine wash

Drierite

front 30

Lab#4

After a recrystallization, a pure substance will ideally appear as a network of _______. If this is not the case, it may be worthwhile to reheat the flask and allow the contents to cool more ______.

back 30

large crystals, slowly

front 31

In order to dissolve a chemical sample in a recrystallization solvent, add the room- temperature solvent _________ in a Erlenmeyer flask on a hot plate. Turn on the heat, starting at ___________. Using a _____, add additional solvent from a second container on the heat source. Swirl the sample flask after each addition, and try to add __________ in order to dissolve the solid.

back 31

just until it covers the sample

a low setting and increasing gradually

pipet

as little solvent as possible

front 32

What property is the basis of the purification technique recrystallization?

back 32

Solubility

front 33

After a mixture has been poured through filter paper, the ______ component remains on top while the _____ flows through. To collect the solid, spread the filer paper _______ and allow the solvent to ______.

back 33

solid, liquid, on a watch glass, evaporate.

front 34

After assembling a gravity filtration apparatus, begin the separation of the mixture by _____ it into the filter paper. Pour the entire contents of the mixture into the filter paper, ______ the solid in the filter paper if needed to speed up filtration. After all the liquid has drained through the filter paper, finish by rinsing the solid with ______.

back 34

decanting, stirring, solvent.

front 35

Using letters on the imagine, identify each component of the vacuum filtration set up.

back 35

A - Clamp

B - Side-arm flask

C - Buchner funnel

D - Adapter

E - Vacuum tubing

front 36

You can separate a mixture of sand and copper(II) sulfate pentahydrate using filtraton. What difference in properties enables the separation of the two solids by filtration?

back 36

The hydrate is soluble in water but the sand is not.

front 37

Sulfuric acid, H2SO4, is an important industrial chemical, typically synthesized in a multi-step process. What is the percent yield if a batch of H2SO4 has a theoretical yield of 3.6 kg, and 2.7 kg are obtained at the end of the process?

back 37

75%

percent yield = actual yield / theoretical yield x 100%

front 38

Why might activated carbon be added to a sample during the recrystallization process?

back 38

To absorb impurities causing the recrystallization solution to have an incorrect color.

front 39

When using vacuum filtration to separate a dissolved solid from an undissolved solid, what techniques should you use to ensure a a quantitative separation?

back 39

-> Dry the solid on the filter paper after the separation

-> Wet the filter paper before pouring the mixture into the filter funnel.

front 40

Lab#5

At the melting point, the solid form of a substance _________ the liquid form of the substance.

back 40

is in equilibrium with

front 41

1. Experimental melting point is close to literature value____

2. Experimental melting point is below literature value_____

3. Wide melting point range_____

4. Narrow melting point range______

back 41

1 & 4 : Pure sample of a single compound

2 & 3 : Impure sample of multiple compounds.

front 42

To prepare a sample in a capillary tube for a melting point determination, gently tap the tube into the sample with _____ end of the tube down. Continue tapping until the sample is ________ . Then, with the _____ end of the tube down, tap the sample down slowly or ____________ to move the sample down faster.

Finally, make sure that you can see _________ in the magnifier when placed in the melting point apparatus before turning on the heat.

back 42

open

couple of millimeters high

closed, drop the tube into a longer tube

some or all of the solid

front 43

Why should you use a finely ground solid when determining the melting point of a sample?

back 43

-> Air pockets in a coarse sample could disrupt heat distribution.

-> Uniform, small particles heat more consistently throughout the sample.

front 44

What characteristics should a good sample for melting point determination have?

back 44

-> Solid phase

-> Thoroughly dry

-> Small particles

front 45

What is the recommended order of measurements to report the most accurate melting point possible?

Use quick heating to estimate the melting point _____

Use slow heating to carefully observe melting _____

Use slow heating to confirm the careful measurement ____

back 45

First step

Second step

Third step

front 46

When performing a melting point determination, how should you report your findings?

back 46

As a rang from the temperature when melting starts to the temperature when it ends.

front 47

When melting mixtures of compounds, what is the eutectic composition?

back 47

The mixture composition with the lowest melting point.