Topic 5 (Alkene mechanisms and Polymers)

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16 Terms

1
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for mechanism of (asymmetric) alkene reacting with HBr/HCl/HF, where does Br attack to form major product?

  • for major products, they will attack the most stable carbocation, or the carbon bonded to more carbons
    (hydrogen bonds to the other less stable Carbocation)


<ul><li><p><strong><u>for major products</u></strong>, they will attack the most stable carbocation, or the carbon bonded to more carbons<br>(hydrogen bonds to the other less stable Carbocation)</p></li></ul><p></p>
2
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alkyl groups are _____

alkyl groups are electron giving groups, always gives electron to carbocation

3
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<p>What does the curly arrows shown represent ?</p>

What does the curly arrows shown represent ?

movement of pair of electron from a bond to an atom, forming ion

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<p>bromine water test (add bromine solution)</p>

bromine water test (add bromine solution)

propane = remains orange solution
(substitution)

propene = turns colorless
(as an alkene undergoes addition with bromine and thus makes solution colorless)

NOTE:
for both test for alkane and alkene → two layer forms
( bottom water and top orange if alkane/ colorless if alkene )

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<p></p>
6
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what feature of pi bond allows sterioisomerism (E Z )

π bond gives restricted rotation around the C=C double bond.

7
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complete combusion products and incomplete combustion products

CxHy + O2 → CO2 + H20

CxHy + O2 → C + H20 [ OR CO + H20]

8
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Describe 2 differences between orbital overlap of sigma and pi bond between carbon atoms

  • sigma bond has 1 area of orbital overlap(or electron cloud) but pi bond has 2

  • sigma bond has head on overlap but pi bond has sideways overlap



(look at diagram, sigma has 1 area of orbital overlap while pi got 2)

<ul><li><p>sigma bond has <strong><u>1 area of orbital overlap</u></strong>(or electron cloud) but <strong><u>pi bond has 2</u></strong><br></p></li><li><p>sigma bond has <strong><u>head on overlap</u></strong> but pi bond has<strong><u> sideways overlap</u></strong></p></li></ul><p><br><br>(look at diagram, sigma has 1 area of orbital overlap while pi got 2)</p>
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pi bond from C=C broken and sigma bond from H-H is broken


sigma bond formed between C-H

<p>pi bond from C=C broken and sigma bond from H-H is broken </p><p></p><p>sigma bond formed between C-H</p>
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NOTE:

stability of compound does not determine which product is formed, rather it is the stabitlity of carbocation

<p>NOTE:</p><p>stability of compound does not determine which product is formed, rather it is the stabitlity of carbocation</p>
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What reagent and condition is needed to make chloroethane from ethane

reagent = chlorine /Cl2
condtion = UV light

12
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why does making chloroethane with ethene give more percentage yield than with ethane

it is an addition reaction that producesonly one product

13
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give 3 factors that need to be considered before deciding which aterial to use such as metal and PVC for long term sustainable use.

  • biodegradeable

  • availability

  • renewable or non-renewable source


14
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what is an electrophile?

define free radical

a species that can accept a pair of electrons to form covalent bond
(species that is attracted to a region of high electron density)

Free radical is a species that contains an unpaired electron

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<p>The mechanisms shown of ther reaction is an example of what?</p>

The mechanisms shown of ther reaction is an example of what?

electrophilic addition

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name the mechanisms:

alkane + halogen

alkene + halogen

alkane + halogen = free radical substitution

alkene + halogen = electrophilic addition