![When methyl vinyl ether reacts with a strong acid, the proton adds to C2 exclusively, instead of C1 or the oxygen atom. Draw the three protonated forms of methyl vinyl ether and When methyl vinyl ether reacts with a strong acid, the proton adds to C2 exclusively, instead of C1 or the oxygen atom. Draw the three protonated forms of methyl vinyl ether and](https://homework.study.com/cimages/multimages/16/6693744-recreated6356257582174964789.png)
When methyl vinyl ether reacts with a strong acid, the proton adds to C2 exclusively, instead of C1 or the oxygen atom. Draw the three protonated forms of methyl vinyl ether and
![2-Chloroethyl vinyl ether, ca. 95%, Thermo Scientific Chemicals, Quantity: 100 g | Fisher Scientific 2-Chloroethyl vinyl ether, ca. 95%, Thermo Scientific Chemicals, Quantity: 100 g | Fisher Scientific](https://assets.fishersci.com/TFS-Assets/CCG/Chemical-Structures/chemical-structure-cas-110-75-8.jpg-650.jpg)
2-Chloroethyl vinyl ether, ca. 95%, Thermo Scientific Chemicals, Quantity: 100 g | Fisher Scientific
Living carbocationic polymerization of a vinyl ether monomer derived from soybean oil, 2-(vinyloxy)ethyl soyate - Green Chemistry (RSC Publishing)
![Expanding vinyl ether monomer repertoire for ring‐expansion cationic polymerization: Various cyclic polymers with tailored pendant groups - Kammiyada - 2017 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library Expanding vinyl ether monomer repertoire for ring‐expansion cationic polymerization: Various cyclic polymers with tailored pendant groups - Kammiyada - 2017 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/b40c97dd-1a5f-4cd3-9749-0cda80cfa3e5/pola28648-fig-0002-m.jpg)