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Explain why methyl vinyl ether (CH2=CHOCH3) is not a reactive dienophile in the Diels-Alder reaction. | Homework.Study.com
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Living cationic polymerization of α‐methyl vinyl ethers using SnCl4 - Yonezumi - 2008 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library
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Synthesis of poly(vinyl ether) plastics for optical use by cationic copolymerization of tricyclodecyl vinyl ether with n‐butyl vinyl ether - Namikoshi - 2007 - Journal of Polymer Science Part A: Polymer Chemistry -
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Pd-Catalyzed Three-Component Reaction of Anilines, Ethyl Vinyl Ether, and Nitro-Paraffin: Assembly of β-Nitroamines | Organic Letters
![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
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