Question

Combine 0.925 grams of 4-(diethylamino)salicyaldehyde (1.0 equivalent), ethyl acetoacetate (7.65 equivalents) and piperidine (1.95 equivalents) in...

Combine 0.925 grams of 4-(diethylamino)salicyaldehyde (1.0 equivalent), ethyl acetoacetate (7.65 equivalents) and piperidine (1.95 equivalents) in a 50 mL round bottom flask with stirring.

What quantity of ethyl acetoacetate do you need to add? Enter a quantity accurate to three significant figures. For liquids, enter a volume in millilitres (mL). For solids, enter a mass in grams (g).

Quantity of ethyl acetoacetate =

What quantity of piperidine do you need to add? Enter a quantity accurate to three significant figures. For liquids, enter a volume in millilitres (mL). For solids, enter a mass in grams (g).

Quantity of piperidine =

If you isolate 0.695 g at the end of your purification, what is your experimental yield? Enter a percentage accurate to three significant figures.  

Experimental yield =

Use a quantity table with MW, quantity, density, moles, and equivalents to show values and calculations

0 0
Add a comment Improve this question Transcribed image text
Know the answer?
Add Answer to:
Combine 0.925 grams of 4-(diethylamino)salicyaldehyde (1.0 equivalent), ethyl acetoacetate (7.65 equivalents) and piperidine (1.95 equivalents) in...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • Just Answer Question 5 Synthesis of 2-chloro-2-methylbutane (literature version) Concentrated aqueous hydrochloric acid (HCI, 3.3 equivalents)...

    Just Answer Question 5 Synthesis of 2-chloro-2-methylbutane (literature version) Concentrated aqueous hydrochloric acid (HCI, 3.3 equivalents) was slowly added to 2-methyl-2-butanol (1.0 equivalents) in a 100 mL round bottom flask with stirring. The reaction was stirred for 15 minutes at room temperature. Upon completion, the reaction mixture was transferred to a 60 mL separatory funnel and the aqueous layer was removed. The organic layer (i.e. the product) was successively washed with: (1) saturated aqueous NaCl (brine), (2) saturated aqueous NaHCO,...

  • What is the theoretical yield (in grams) and percent yield of your triphenylmethanol product in this...

    What is the theoretical yield (in grams) and percent yield of your triphenylmethanol product in this experiment? (Weight of triphenylmethanol: 0.060g) BACKGROUND AND THEORY The Grignard reaction was one of the first organometallic reactions discovered and is still one of the most useful synthetically. By reacting an organohalide (usually a bromide) with magnesium in ethereal solvent, carbon becomes a nucleophile. Grignard reagents are the starting points for the syntheses of many alkanes, primary, secondary, and tertiary alcohols, alkenes, and carboxylic...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT