Aromatic Chemistry Flashcards

1
Q

State, in terms of its bonding, why benzene is more stable than
cyclohexa−1,3,5−triene

A

Electrons delocalised

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2
Q

Explain your answers to part (i) and part (ii) in terms of the bonding in these
two dienes. (cyclohexa-1,3-diene and cyclohexa-1,4-diene)

A

-Proximity − for 1,3 C=C bonds are close together
-Proximity − for 1,3 C=C bonds are close together
-some extra stability for the 1,3- isome

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3
Q

What is empirical formula?

A

The simplest whole number ratio of atoms present in a compound.

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4
Q

What is the reducing reagent for the conversion of a nitrobenzene to a phenylamine?

A

-HCl

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5
Q

What is the reducing reagent for the conversion of benzene to cyclohexane?

A

-H2

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6
Q

What is the bond angle between the carbon atoms of benzene?

A

-120 degrees

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7
Q

What is the bond angle between the carbon atoms of cyclohexane?

A

-109.5 degrees

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8
Q

Why would a product be optically inactive?

A

-planar C=O bond
-the attack is equally likely from either side
-a racemic mixture is formed

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9
Q

What is an arene?

A

-a molecule that contains a benzene ring

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10
Q

What is the catalyst for acylation of a benzene ring?

A

-AlCl3

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11
Q

What is necessary for the nitration of benzene?

A

-heat conc HNO3
-with H2SO4

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12
Q

What is the bond length of C-C bonds in a benzene molecule?

A

-139pm

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