Activity No. 1 Flashcards

1
Q

one of the general methods available for making alkyl halides

A

nucleophilic substitution reactions

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2
Q

halides sources that are applicable only for the preparation of primary halides but not for tertiary alkyl halides because elimination reactions predominate

A

phosphorous trihalides or thionyl halides

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3
Q

the halogen acid employed in the experiment which reacts readily w/ tert-butyl

A

hydrochloric acid

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4
Q

in the first stage of the reaction, what is formed?

A

intermediate carbocation

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5
Q

the intermediate carbication formed is stabilized by _________ and _______

A

hyperconjugation
inductive effects

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6
Q

SN1 reaction mechanism is also known as

A

Unimolecular Nucleophilic Substitution

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7
Q

since the tert-butyl chloride product has been in contact with water, it is regarded as _______, hence, it needs a ________

A

wet
drying agent

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8
Q

it is usually an inorganic compound that reacts irreversibly with water, or that is capable of forming one or more hydrates

A

drying agent

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9
Q

why must we be careful in selecting a drying agent

A

to avoid forming a complex withbthe organic compound or solvent, or react in some other way

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10
Q

what are the more commonly used drying agents?

A

calcium chloride (CaCl2)
magnesium sulfate (MgSO4)
sodium sulfate (Na2SO4)

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11
Q

specifically what drying agent will be used in the experiment?

A

calcium chloride (CaCl2)

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12
Q

In the experiment, why does CaCl2 was employed?

A

because of its fast action amd high capacity to remove water

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13
Q

in drying, where must be the wet liquid be placed?

A

in an Erlenmeyer flask, sealed with a cork

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14
Q

basis for the “appropriate amount” of drying agent to be added

A

if the amount added covers the bottom of the flask

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15
Q

swirling the mixture (increases/decreases) the rate of drying.

A

increases

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16
Q

what is the minimum time for thorough drying

A

an HOUR of contact between the liquid and the drying agent

17
Q

the product tert-butyl chloride is mainly used as an

A

alkylating agent

18
Q

a chemical used in this experiment that is corrosive and a poison

A

Concentrated HCl

19
Q

TRUE/FALSE.
Both alcohol and alkyl halide are flammable

A

TRUE

20
Q

reaction between the residual HCl and NaHCO3 will give off a sufficient amount of ____

A

CO2

21
Q

dry the organic layer over _______

A

anhydrous CaCl2

22
Q

the drying agent will be removed by ______

A

decantation

23
Q

what indicates that a reaction has taken place between the alkyl halide and AgNO3

A

appearance oof a white precipitate

24
Q

1st step in the procedure

A

Put 5 mL of t-butyl alcohol in a 50mL Erlenmeyer flask and place the flask over a motor stirrer, then add a stir bar and start stirring

25
Q

2nd step in the procedure

A

Add 13mL of concentrated HCl (12N) . Stir the mixture for 15mins or until the solution becomes colorless

26
Q

step 3 in the procedure

A

transfer the mixture to a 100mL separatory funnel and allow to stand until two clear layers have separated

27
Q

4th step in the procedure

A

remove the aqueous layer then wash the organic layer with 6mL of saturated aqueous NaCl solution

28
Q

5th Step

A

then wash the organic layer with 6mL of saturated aqueous NaHCO3 solution

29
Q

Step 6 in the procedure

A

wash the organic layer with another 6mL of saturated aqueous NaCl. Then save the organic layer

30
Q

The reaction between residual HCl and NaHCO3 gives off sufficient amount of CO2. Care must be taken NOT to confine this gas in the funnel. So, what must be done next?

A

Swirl the mixture initially in the UNSTOPPERED upright funnel, then invert the funnel and vet IMMEDIATELY into the hood

31
Q

How long will you gently and briefly shake the funnel between periods of venting?

A

until the evolution of gas subsides