Haloalkanes Flashcards

1
Q

Trend of BP of haloalkanes?

A

INCREASES down group

  • atomic radius increases
    = stronger instantaneous-induced forces between mol. –> more energy to overcome
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2
Q

The carbon-halogen bond in haloalkanes is____. Why?

A

POLAR

  • halogens more ELECTRONEGATIVE than C
  • halogen pulls e- density away from C so it’s e- deficient
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3
Q

What is a nucleophile?

A

Electron-pair donor

*donates electron pair to somewhere without enough electrons

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4
Q

Examples of nucleophiles?

A

OH- NH3 H2O

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5
Q

What is a substitution reaction?

A

When a FUNCTIONAL GROUP in compound is replaced by another functional group

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6
Q

What happens in a nucleophile company substitution reaction?

A

Nucleophile attacks a δ+ carbon and replaces the δ- atom/group

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7
Q

Haloalkanes react with _____ ___ by nucleophiles reaction

A

Hydroxide ions

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8
Q

General equation for haloalkanes undergoing nucleophilic substitution

A

R-X + NaOH –> ROH + NaX

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9
Q

Warming a haloalkanes with _____ also results in nucleophilic substitution

A

water

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10
Q

What are amines?

A

Based on ammonia (NH3) but 1+ of the H atoms replaced by ALKYL groups

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11
Q

What is a haloalkane?

A

Alkane with at least one HALOGEN atom in place of a H atom

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12
Q

Why are iodoalkanes the most reactive haloalkanes?

A

Even tho C-F bond is most POLAR - it’s the strongest = highest bond enthalpy = slower reaction

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