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Explain alkanoates. 2. State any three members of the alkanoate family. 3. Explain esterification. 4. Write a typical equation representing esterification. 5. Differentiate between polymerisation and condensation. What is the difference between alkalis and bases?

Chemistry

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(1) Addition polymerization of alkenes

Addition polymerization of alkenes is a chain-growth process where multiple alkene molecules (monomers with C=C double bond) link together by opening the double bond, forming a long chain polymer without loss of any small molecule byproduct.

Typical mechanism: Free radical addition polymerization.

General reaction for ethene (a common alkene):

n CH2=CH2→initiator[−CH2−CH2−]nn \ \mathrm{CH_2=CH_2} \xrightarrow{\text{initiator}} \left[ -\mathrm{CH_2-CH_2}- \right]_n

Steps:

  • Initiation: Peroxide initiator decomposes to radicals.
(R−O)2→2 R−O∙\mathrm{(R-O)_2} \rightarrow 2 \ \mathrm{R-O^\bullet} R−O∙+CH2=CH2→R−O−CH2−CH2∙\mathrm{R-O^\bullet + CH_2=CH_2 \rightarrow R-O-CH_2-CH_2^\bullet}
  • Propagation: Radical adds to monomer repeatedly.
R−O−(CH2−CH2)n∙+CH2=CH2→R−O−(CH2−CH2)n+1∙\mathrm{R-O-(CH_2-CH_2)_n ^\bullet + CH_2=CH_2 \rightarrow R-O-(CH_2-CH_2)_{n+1} ^\bullet}
  • Termination: Radicals combine.
R−O−(CH2−CH2)m∙+R−O−(CH2−CH2)p∙→R−O−(CH2−CH2)m+p−O−R\mathrm{R-O-(CH_2-CH_2)_m ^\bullet + R-O-(CH_2-CH_2)_p ^\bullet \rightarrow R-O-(CH_2-CH_2)_{m+p}-O-R}

Three monomers (alkenes): Ethene (CH2=CH2\mathrm{CH_2=CH_2}), propene (CH2=CH−CH3\mathrm{CH_2=CH-CH_3}), but-1-ene (CH2=CH−CH2−CH3\mathrm{CH_2=CH-CH_2-CH_3}).

(2) Chain reaction representing typical homopolymer situation

Homopolymer: Polymer formed from one type of monomer only.

Typical situation: Free radical addition polymerization of an alkene (e.g., ethene to polyethylene).

Chain reaction has three main steps:

Initiation:

Peroxide decomposes:

Bz2O2→2 BzO∙(Bz=C6H5CH2)\mathrm{Bz_2O_2} \rightarrow 2 \ \mathrm{BzO^\bullet} \quad (\mathrm{Bz = C_6H_5CH_2})

Radical adds to monomer:

\mathrm{BzO^\bullet + CH_2=CH_2 \rightarrow \mathrm{BzO-CH_2-CH_2^\bullet}

Propagation:

\mathrm{BzO-CH_2-(CH_2-CH_2)_{n-1}-CH_2 ^\bullet + CH_2=CH_2 \rightarrow \mathrm{BzO-CH_2-(CH_2-CH_2)_n -CH_2 ^\bullet}

Termination (combination):

\mathrm{BzO-(CH_2-CH_2)_m ^\bullet + \mathrm{BzO-(CH_2-CH_2)_n ^\bullet \rightarrow BzO-(CH_2-CH_2)_{m+n}-OBz}

This represents homopolymerization as only one monomer (ethene) is used.

(3) Difference between polymerization and condensation

Polymerization (Addition)Condensation
Monomers link by addition across multiple bond (e.g., C=C).Monomers link by elimination of small molecule (e.g., H2_2O).
No byproduct.Byproduct formed.
Chain-growth, fast.Step-growth, slower.
Example: n CH2=CH2→[−CH2−CH2−]nn \ \mathrm{CH_2=CH_2} \rightarrow [\mathrm{-CH_2-CH_2-}]_n (polyethene).Example: HO-(CH2_2)4_4-OH + HOOC-(CH2_2)4_4-COOH →\rightarrow [-O-(CH2_2)4_4-OOC-(CH2_2)4_4-CO-]n_n + (2n-1) H2_2O (nylon 6,6).

Difference between homopolymers and copolymers

Homopolymers: Formed from a single type of monomer. All repeating units identical.

Example: Polyethene [−CH2−CH2−]n[\mathrm{-CH_2-CH_2-}]_n from ethene only.

Copolymers: Formed from two or more different monomers. Repeating units vary.

Example: Styrene-butadiene rubber (SBR): [-CH(CH3_3)-CH2_2-] from propene? Wait, styrene C6H5CH=CH2\mathrm{C_6H_5CH=CH_2} and buta-1,3-diene CH2=CH−CH=CH2\mathrm{CH_2=CH-CH=CH_2}.

Types of copolymers: Random, alternating, block, graft.

See above explanations

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