Chapter 3 - Alkenes and Alkynes Flashcards

1
Q

What type of hydrocarbons are alkenes and alkynes?

A

Unsaturated

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2
Q

General formula for alkenes

A

CnH2n

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3
Q

General formula for alkynes

A

CnH2n-2

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4
Q

General formula for saturated hydrocarbon

A

CnH2n+2

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5
Q

Alkadienes that are separated by one C-C single bond

A

Conjugated

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6
Q

Alkadienes that are separated by more than one C-C single bond)

A

Nonconjugated

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7
Q

True or False:

carbon–carbon double bonds are longer than carbon–carbon single bonds

A

False
(Shorter)

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8
Q

bond is formed from the end-on overlap of two orbitals

A

Sigma

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9
Q

bond is formed by lateral overlap of p orbitals on adjacent atoms

A

Pi

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10
Q

Reaction that is common for alkanes

A

Substitution

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11
Q

Reaction common for alkenes

A

Alkenes

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12
Q

True or False:

sigma bonds are usually stronger than pi bonds

A

True

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13
Q

Test for unsaturation

A

Bromine test

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14
Q

Water adds as H-OH in hydration and the products are what?

A

Alcohols

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15
Q

It gives only one of the two possible regioisomers

A

Regiospecific

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16
Q

It produces mainly one regioisomer

A

Regioselective

17
Q

The only product for regiospecific

A

2-propanol

18
Q

electron-poor reactants; they seek electrons.

A

Electrophiles

19
Q

electron-rich reactants; they form bonds by donating electrons to electrophiles.

A

Nucleophiles

20
Q

act as a supplier of pi electrons to an electron-seeking reagent

A

Double bond

21
Q

A positively charged carbon atom bonded to three other atoms

A

Carbocation

22
Q

What rule is this?

The electrophilic addition of an unsymmetric reagent to an unsymmetric double bond proceeds in such a way as to involve the most stable carbocation.

A

Markovnikov’s rule

23
Q

It shows the changes in energy that occur in the course of a reaction

A

Reaction energy diagram

24
Q

A structure with maximum energy for a particular reaction step

A

Transition state

25
Q

It is the difference in energy between reactants and the transition state and determines the reaction rate.

A

Activation energy

26
Q

True or False:

Higher the energy barrier, the faster the reaction

A

False
(Higher the energy barrier, the slower the reaction)

27
Q

Addition of H-B to an alkene

A

Hydroboration

28
Q

Addition of hydrogen to alkenes in the presence of a catalyst

A

Hydrogenation

29
Q

Carbocation with a carbon–carbon double bond that is adjacent to the positively charged carbon atom

A

Allylic cation

30
Q

the cycloaddition reaction of a conjugated diene and a dienophile to give a cyclic product in which three  bonds are converted to two  bonds and a new  bond.

A

Diels-Alder reaction

31
Q

True or False:

Alkenes react rapidly and quantitatively with ozone

A

True

32
Q

It can be used to locate the position of a double bond.

A

Ozonolysis

33
Q

Angle betweem teo sp orbitals of a triple bond

A

180 degrees

34
Q

True or False

hydrogen atom on a triply bonded carbon is weakly basic

A

False
(Weakly acidic)

35
Q

The process of polymer formation

A

Polymerization