chapter 14 - alkenes Flashcards

1
Q

What is the definition of structural isomerism

A

Molecules with the same molecular formula but a different structural formula.

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2
Q

What is the definition of stereo isomerism

A

Molecules with the same molecular and structural formulas but a different arrangement of the items in space

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3
Q

How does stereo E-Z isomerism form

A

The double carbon carbon bond has a restricted rotation of each carbon and this gives rise to geometric isomerism

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4
Q

What is E-isomerism

A

When the priority group is not on the same side

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5
Q

what is Z-isomerism

A

When the priority group is on the same side (Z same) zame

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6
Q

What is the definition of a position isomer

A

It has the same molecular formula but a different position of the functional group

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7
Q

What is the definition of a chain Isomer

A

It has the same molecular Formula but a different arrangement of the carbon chain

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8
Q

What is functional group isomerism

A

It has the same molecular formula but a different functional group

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9
Q

What is a sigma bond

A

A sigma bond Is where there are electrons between the two carbon atoms

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10
Q

what is a pi bond

A

A covalent bond where electrons are above and below the plane of the 6 central atoms. formed from an overlap of p orbitals on the C atoms.

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11
Q

How do you classify Cabocations

A

tertiary carbocations will have 3 R groups

secondary carbocations will have 2 R groups

a primary carbocation will have 1 R group

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12
Q

which carbocation is the most stable

A

tertiary is the most

secondary

primary is the least

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13
Q

why does having more R groups make a carbocation more stable?

A

R groups can donate electron density onto the positive carbon. making the cation more stable

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14
Q

where is the major product formed from in electrophillic addition

A

from the most stable carbocation

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15
Q

Where do the arrows go in an electrophilic addition mechanism (not sulfuric acid)

A

from the double bond onto the H or more + element.

from the middle of the H-Br bond for example onto the Br

from the middle of the lone pair on the bromine onto the most stable carbocation.

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16
Q

where do the arrows go in electrophillic addition of H2SO4(strong acid)

A

draw it as H-OSO3H

double bond to the H on H-OSO3H

from the middle of that bond onto the OSO3H

from the middle of the lone pair of OSO3H to the positive carbon.

to name this molecule, you would name it as propyl/butyl hydrogen sulfate

17
Q

Where do the arrows go in the electrophilic addition reaction with water (H2O)

A

reagent( strong acid, H2SO4 or H3PO4 )

from the double bond to a single hydrogen (H+)

from the lone pair on water to the positive carbon (carbocation)

from the O-H bond onto the positive O

hydrogen (H+) acts as a catalyst in this reaction

18
Q

naming alkenes

A

if there are two double bonds. you have to state where each double bond is. eg hexA-2,4-DIene

19
Q

hydrogenation/reduction mechanism. H2

A

conditions - Nickel, 150°C [NI]

eg. CH2=CH2 + H2 = CH3CH3

20
Q

hydration mechanism H2O

A

conditions. 65atm, 300°C, concentrated H3PO4, phosphoric acid

CH2=CH2 + H2O = CH3CH2OH

Industrial method for making ethanol

21
Q

Addition polymerization reaction

A

Conditions- Organic peroxide initiator or other catalyst

eg CH2=CH2 = broken double bond and square brackets with an n in the bottom right corner.

Two forms are made [LDPE] low density polyethene, and [HDPE] high density polyethene

22
Q

how can alkenes contain permanent dipole dipole forces

A

if they are a Z isomer. electrons can pile up on one side of the molecule creating a dipole. slightly delta negative region and a slightly delta positive region