Topic 17- Organic II Flashcards

1
Q

What is a chiral object?

A

A molecule that has non-super imposable on its mirror image

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2
Q

What are the key features of a chiral centre

A

A carbon bonded to 4 different groups

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3
Q

Optical activity

A

The ability of a single isomer to rotate on the plane of plane-polarised light

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4
Q

What is a racemic mixture?

A

50/50 mix of two different isomers which will cancel each other out and become optically inactive

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5
Q

What intermediate takes place in Sn1

A

Carbocation intermediate

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6
Q

What intermediate takes place in Sn2

A

Transition state

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7
Q

What are the conditions for the reaction between a carbonyl compound and hydrogen cyanide

A

Acidic conditions

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8
Q

What is a test for the CH3CO group?- observations?

A

carbonyl with warmed alkaline iodine
-forms a pale yellow precipitate

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9
Q

Colour change of acidified potassium dichromate if aldehyde present

A

orange to green

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10
Q

Colour change of Fehlings solution if aldehyde present

A

deep blue to red

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11
Q

Observation for Tollens Reagent for aldehydes

A

colourless to silver mirror

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12
Q

Reducing agent for reduction of aldehyde and ketones to alcohols?

A

LiAlH4- Lithium Aluminium Hydride
- dry ether conditions

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13
Q

Colour of precipitate from Bradys reagent with carbonyl group?

A

orange precipitate

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14
Q

How to identify different carbonyl compounds from derivates of Bradys reagent?

A

-filtered, purified and dried
- compare melting temperatures with data booklet

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15
Q

Why can the reaction between HCN and a carbonyl be optically inactive?

A

due to the C=O bond being planar, nucleophile can attack from above and below forming a racemic mixture

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16
Q

Why do carboxylic acids have high boiling points?

A

-three polar bonds include hydrogen bonding in O-H group, permanent dipole-dipole interactions and London forces

17
Q

What can short chain carboxylic acids form?

A

dimers - double molecules
carboxylic acids can hydrogen bond with each other