| 21. | The iodide leaving group in methyl iodide may cause side reactions, as it is a powerful nucleophile.
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| 22. | Several side reactions are known to occur.
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| 23. | The ?-hydride elimination can either be a vital step in a reaction or an unproductive side reaction.
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| 24. | Another side reaction is the Tishchenko reaction.
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| 25. | The use of solvents with low-dielectric constants such as dichloromethane or chloroform can minimize this side reaction.
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| 26. | :Side reactions will occur on my electrophile-- it's a condensed amino acid with substituted groups on it.
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| 27. | A side reaction is an unwanted chemical reaction taking place that diminishes the yield of the desired product.
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| 28. | Side reactions decrease the current efficiency.
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| 29. | These side reactions can be reduced by only short exposures to the catalyst of the order of 0.0003s.
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| 30. | Inevitably, [ 4 + 4 ] photocycloadditions carry the side reaction of [ 2 + 2 ] photocycloadditions.
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