1)Explain using drawings why acetaldehyde reacts faster than acetone to nucleophilic acyl addition.
2)
3)What is the major purpose of pyridine in nucleophile acyl substitution reactions (for example, a reaction including an acid chloride with pyridine)?
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1)Explain using drawings why acetaldehyde
reacts faster than acetone to nucleophilic acyl addition.
2)
3)What is...
Explain using drawings why acetaldehyde reacts faster than acetone to nucleophilic acyl addition. For partial credit...
Explain using drawings why acetaldehyde reacts faster than acetone to nucleophilic acyl addition. For partial credit draw acetaldehyde and acetone
Question 12 6 pts Explain using drawings why acetaldehyde reacts faster than acetone to nucleophilic acyl...
Question 12 6 pts Explain using drawings why acetaldehyde reacts faster than acetone to nucleophilic acyl addition. Include your answer sheet upload to Canvas in the Assignments folder or email your answer to Dr. Berger. Note: there may be more than one way to answer this question. Only one correct explanation is required. For partial credit draw acetaldehyde and acetone
i. What is the purpose of the cyclic acetal in the following reaction? ii. Draw the...
i. What is the purpose of the cyclic acetal in the following reaction? ii. Draw the product formed if the original starting material was treated with 1. LiAIH4 & 2. H20 (i.e. what would happen if the 1st and 3rd reactions were not performed?) O O O 1. LiAlH, O H,0 OH OH Glycerol TSOH OH 2. H2O OH
i. What is the purpose of the cyclic acetal in the following reaction? ii. Draw the...
i. What is the purpose of the cyclic acetal in the following
reaction?
ii. Draw the product formed if the original starting material
was treated with 1. LiAlH4 & 2. H2O (i.e.
what would happen if the 1st and 3rd reactions were not
performed?)
о о о о о Glycerol 1. LiAIH, о H,O* ОН ОН ОН он TOH 2. H2O
Paragraph Styles 6. ... 7 1. Why is an ester less reactive to nucleophilic acyl substitution...
Paragraph Styles 6. ... 7 1. Why is an ester less reactive to nucleophilic acyl substitution than an acid chloride? A) Chloride is a better leaving group B) Oxygen is better at donating electron density into the carbonyl with added resonance stability. C) Chloride is a better leaving group and compared to chlorine, oxygen is better at donating electron density into the carbonyl with added resonance stability D) The alkoxy anion is less basic than the chloride anion. 2. What...
Question 12 6 pts Explain using drawings why acetaldehyde reacts faster than acetone to nucleophilic acyl addition. Include your answer sheet upload to Canvas in the Assignments folder or email your answer to Dr. Berger. Note: there may be more than one way to answer this question. Only one correct explanation is required. For partial credit draw acetaldehyde and acetone
i. What is the purpose of the cyclic acetal in the following reaction? ii. Draw the product formed if the original starting material was treated with 1. LiAIH4 & 2. H20 (i.e. what would happen if the 1st and 3rd reactions were not performed?) O O O 1. LiAlH, O H,0 OH OH Glycerol TSOH OH 2. H2O OH
i. What is the purpose of the cyclic acetal in the following
reaction?
ii. Draw the product formed if the original starting material
was treated with 1. LiAlH4 & 2. H2O (i.e.
what would happen if the 1st and 3rd reactions were not
performed?)
о о о о о Glycerol 1. LiAIH, о H,O* ОН ОН ОН он TOH 2. H2O
Paragraph Styles 6. ... 7 1. Why is an ester less reactive to nucleophilic acyl substitution than an acid chloride? A) Chloride is a better leaving group B) Oxygen is better at donating electron density into the carbonyl with added resonance stability. C) Chloride is a better leaving group and compared to chlorine, oxygen is better at donating electron density into the carbonyl with added resonance stability D) The alkoxy anion is less basic than the chloride anion. 2. What...
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