Cyclic Acetal Protecting Group Reaction and Mechanism
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Cyclic Acetal Protecting Group Reaction and Mechanism
Forming cyclic acetal protecting groups can be tricky! Watch the step-by-step detailed mechanism. You'll also see tips about redrawing, and a time saving shortcut to use during practice and your upcoming exam! Part of a full video series on Acetals!
Jun 17, 2021
Acetal Synthesis
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Devise a synthesis of each acetal from 1-bromo-2-methylhexane, alcohols (and diols) containing one or two carbons, and any needed inorganic reagents. | Numerade
Devise a synthesis of each acetal from 1-bromo-2-methylhexane, alcohols (and diols) containing one or two carbons, and any needed inorganic reagents. | Numerade
numerade.com
Mar 6, 2021
Devise a synthesis of each acetal from 1-bromo-2-methylhexane, ... | Filo
Devise a synthesis of each acetal from 1-bromo-2-methylhexane, ... | Filo
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SOLVED: Show the steps in the acid-catalyzed formation of acyclic acetal from ethylene glycol.
SOLVED: Show the steps in the acid-catalyzed formation of acyclic acetal from ethylene glycol.
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SOLVED: Bonus: Provide curved arrow mechanism for the formation of the cyclic acetal shown below. Use the curved arrows to indicate the direction of the electrons for each step. Include arrows for the proton transfer steps and the intermediate oxonium ions (oxygen with positive charge).HOCH2CH2OHH2SO4
SOLVED: Bonus: Provide curved arrow mechanism for the formation of the cyclic acetal shown below. Use the curved arrows to indicate the direction of the electrons for each step. Include arrows for the proton transfer steps and the intermediate oxonium ions (oxygen with positive charge).HOCH2CH2OHH2SO4
numerade.com
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SOLVED: Show the steps in the acid-catalyzed formation of acyclic acetal from ethylene glycol.
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numerade.com
SOLVED: Bonus: Provide curved arrow mechanism for the formation of the cyclic acetal shown below. Use the curved arrows to indicate the direction of the electrons for each step. Include arrows for the proton transfer steps and the intermediate oxonium ions (oxygen with positive charge).HOCH2CH2OHH2SO4
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numerade.com
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SOLVED:Outline all steps in the mechanism for the formation of a cyclic acetal from acetone and ethylene glycol (1,2-ethanediol) in the presence of anhydrous HCl.
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SOLVED:Write the structures of the cyclic acetal or ketal derived from each of the following: (a) Cyclohexanone and ethylene glycol (b) Benzaldehyde and 1,3-propanediol (c) Isobutyl methyl ketone and ethylene glycol (d) Isobutyl methyl ketone and 2,2-dimethyl-1,3-propanediol
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