Carobyl Compunds Flashcards

1
Q

What is Stephens Reduction?

A

Nitrile +anhydrous SnCl2 + HCL to form aldehyde

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2
Q

What is Rosemunds Reduction?

A

Acid Chlorides on reduction with Lindlar Catalyst (H2+Pd +BaSO4, Quinolene)

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3
Q

Explain dry distillation process to create Aldehydes /Ketones

A

Preparation of aldehyde:
By dry distillation of calcium format and calcium salts of carboxylic acid. Example: calcium acetate plus calcium form guess I said aldehyde plus CaCO3

Preparation of ketone:
By dry distillation of calcium salts of carboxylic acid.

Example: calcium acetate and dry distillation forms acetone Plus CaCO3

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4
Q

What reaction does carbonyl compounds undergo?

A

Nucleophilic addition reaction

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5
Q

What is the hybridisation and shape of carbon compound in carbonyl group?

A

SP2 hybridisation, planar

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6
Q

What are the two types of ketone

A

Simple ketones and mixed Ketone

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7
Q

What other salt can be used for dry distillation to produce Aldehyde and ketone?

A

Barium salts of carboxylic acid

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8
Q

What all reagents can be used for Rosemunds Reduction?

A

1) Lindlars Catalyst (H2-Pd, BaSO4, Quinolene)
2) Lithium tri-t-butoxy Aluiminium Hydride
3) DiBHAL

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9
Q

And explain preparation methods of carbonyl from alkynes?

A

1) Oxymercuration-Demercuration

Using 1% HgSO4, H2SO4, H2O

2) hydroboration followed by oxidation

Using B2H6/BH3, SYN addition

Instead of diBorane we can use disiamly Borane (SIA)2BH - Exclusively forms propanal

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10
Q

state methods of Carbonyl formation from Alcohols?

A

1) Alcohol + mild reducing reagent
1-degree alc gives Aldehydes
2nd-degree alc gives a ketone

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11
Q

How are Carbonyl prepared from Alkenes?

A

1) Reductive Ozonolysis: Alkene+ O3, DCM, Zn, -H2O, at -78C gives Aldehydes and ketones.
2) With Lemieux reagent (NaIO4, H2O, OSO4, KMnO4)? This directly converts alkenes to ketons and aldehydes without forming glycols

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12
Q

Explain preparation off Ketones by Grignard.

A

Nitriles + RMgX = Ketone + MgNH2

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13
Q

Explain reactions of Acid Cholrides with Alkyl Cadmium.

A

Acid Chloride + CdCl2 = Ketone

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14
Q

Why is RMgX not used with Acid Chlorides?

A

RMgX is not used with acid chlorides because it is so reactive that they will form 3-degree Alcohol. R2Cd is less reactive as it is less Electropositive

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