JoVE Logo

로그인

The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.

Figure1

Alkenes undergo polymerization via a free-radical mechanism involving three steps: initiation, propagation, and termination.

Radicals are generated in the initiation step by heating a small quantity of free-radical initiators such as benzoyl peroxide. The benzoyloxy radical loses CO2 and forms a phenyl radical (Ph·), which adds to the double bond of the alkene to initiate the polymerization process. One of the electrons of the alkene π bond pairs with one electron from the phenyl radical to form a new C–C bond.

Figure2

Figure3

Figure4

In the propagation step, the carbon radical generated in the initiation step adds to another molecule of alkene to generate a new radical. The continuous addition of alkene monomers at the radical site yields the polymer.

Figure5

The termination step of the free-radical mechanism occurs via recombination or disproportionation. In a recombination step, two growing chains form a bond at their radical sites.

Figure6

In termination by disproportionation, a β-hydrogen atom is transferred from one radical to another radical center, resulting in two non-radical products.

Figure7

The free-radical polymerization of ethylene yields low-density polyethylene (LDPE), where the low density is a consequence of significant branching in the polymer chains. Articles made from polymers surround us in various forms, such as food packaging materials, plastic bags, bottles, stationery, and automotive parts.

Tags

Free radical Chain ReactionPolymerizationAlkenesPolymersRepeating UnitAverage Degree Of PolymerizationFree radical MechanismInitiationPropagationTerminationRadicalsInitiatorsBenzoyl PeroxidePhenyl RadicalAlkene Double BondPropagation StepCarbon RadicalAlkene MonomersTermination StepRecombinationDisproportionation

장에서 8:

article

Now Playing

8.2 : Free-Radical Chain Reaction and Polymerization of Alkenes

Reactions of Alkenes

7.6K Views

article

8.1 : 친전자성 첨가물의 위치 선택성-과산화물 효과

Reactions of Alkenes

8.3K Views

article

8.3 : 알켄의 할로겐화

Reactions of Alkenes

15.1K Views

article

8.4 : Alkenes에서 Halohydrin의 형성

Reactions of Alkenes

12.6K Views

article

8.5 : Alkenes의 Acid-Catalyzed Hydration (산성 촉매 수화)

Reactions of Alkenes

13.4K Views

article

8.6 : Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration(산-촉매 수화의 위치 선택성 및 입체화학)

Reactions of Alkenes

8.3K Views

article

8.7 : Oxymercuration-알켄 환원

Reactions of Alkenes

7.4K Views

article

8.8 : Hydroboration-Alkenes의 산화

Reactions of Alkenes

7.6K Views

article

8.9 : Hydroboration의 위치 선택성 및 입체화학(Regioselectivity and Stereochemistry of Hydroboration)

Reactions of Alkenes

8.0K Views

article

8.10 : 알켄의 산화 : 오스뮴 테트라 옥사이드를 사용한 Syn Dihydroxylation

Reactions of Alkenes

9.6K Views

article

8.11 : 알켄의 산화 : 과망간산 칼륨을 사용한 Syn Dihydroxylation

Reactions of Alkenes

10.5K Views

article

8.12 : 알켄의 산화 : 과산화산을 사용한 안티 디하이드록실화

Reactions of Alkenes

5.5K Views

article

8.13 : 알켄의 산화적 분열: Ozonolysis

Reactions of Alkenes

9.7K Views

article

8.14 : 알켄의 환원: 촉매 수소화

Reactions of Alkenes

11.7K Views

article

8.15 : 알켄의 환원: 비대칭 촉매 수소화

Reactions of Alkenes

3.2K Views

JoVE Logo

개인 정보 보호

이용 약관

정책

연구

교육

JoVE 소개

Copyright © 2025 MyJoVE Corporation. 판권 소유