Organometallics. Flashcards

1
Q

What are organometallic compounds?

A

Organometallic compounds are compounds that have a carbon to metal bond.

E.g.

Na:C≡CH (sodium acetylide) NaOCH3 ; sodium methoxide

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2
Q

On an organometallic compound where can you find the negative charge and the positive charge?

A

The negative charge can be found on the carbon.

The positive charge can be found on the metal.

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3
Q

On what organometallic compound does the carbon not have a negative charge?

A

Sodium methoxide. NaOCH3.

The negative charge lies on the oxygen.

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4
Q

Organometallic compounds act as a good source of what?

A

Carbanions.

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5
Q

List the alkyl halides in decreasing order of reactivity?

A

R-I.

R-Br.

R-Cl.

R-F.

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6
Q

How can you prepare an organometallic compound?

A

Alkyl halide + Mg = Organomagnesiumhalide.

C2H5Cl + Mg + Diethyl ether = C2H5MgCl ( ethylmagnesium Chloride).

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7
Q

Grignard reagents act as what?

A

Grignard reagents act as a good source of carbanions.

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8
Q

Alkyl halides are more reactive to magnesium than what?

A

Aryl or vinyl halides.

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9
Q

A Grignard reagent + a formaldehyde gives what?

A

A primary alcohol.

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10
Q

A Grignard reagent + an aldehyde gives what?

A

A secondary alcohol.

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11
Q

A Grignard reagent + a ketone gives what?

A

A tertiary alcohol.

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12
Q

What is the best solvent for synthesising a Grignard reagent?

A

Diethyl ether.

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13
Q

A Grignard reagent + ethylene oxide gives what?

A

A primary alcohol.

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14
Q

A Grignard reagent + carbon dioxide gives what?

A

A carboxylic acid.

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15
Q

What happens if we react a Grignard reagent with a cyclic ester?

A

The ring breaks forming a an alkane with a tertiary alcohol.

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16
Q

What are the steps of converting an alkane to an carboxylic acid, without using a Grignard reagent?

A

Step One:
Conversion of alkane to alkyl halide.

Step 2:
Conversion of alkyl halide to alcohol.

Step 3:
Oxidation of alcohol.

17
Q

What are the steps of converting an alkane to a carboxylic acid, using a Grignard reagent?

A

Step One:
Conversion of alkane to alkyl halide.

Step two:
Conversion of alkyl halide to Grignard’s reagent.

Step three:
Reaction of Grignard Reagent with CO2.

18
Q

How do we add 2 extra carbons on to an alcohol?

A

Step One:
Alcohol to Alkylhalide.

Step Two:
Alkyl halide to Grignard Reagent.

Step three:
Grignard + Ethylene Oxide.

19
Q

How do we add 1 extra carbon on to an alcohol?

A

Step One:
Alcohol to Alkylhalide.

Step Two:
Alkyl halide to Grignard Reagent

Step Three:
Grignard + Formaldehyde.