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Alja [10]
3 years ago
8

Write an equation that shows the reaction between acetic acid and triethylamine (CH3CH2)3N. Draw all non-bonding lone electron p

airs and show the electron flow with curved arrows. QUESTION 4 : Which functional groups are in the structure of Prpstaglandin E1 ?

Chemistry
1 answer:
Anni [7]3 years ago
8 0

Answer:

-) Acid-base reaction

-) Carboxylic acid, alcohol, alkene and ketone

Explanation:

For the reaction between acetic acid and triethylamine, we will have an <u>acid-base reaction</u>. Therefore a s<u>alt would be produced</u> in this case an  <u>"ammonium quaternary salt"</u>. Also, we have to remember that on this reaction the acid is the acetic acid and the base is the triethylamine. See figure 1

For the second question, we have to check the <u>structure of Prostaglandin</u> E1 in which we have the functional groups:

<u>1) Carboxylic acid</u>

<u>2) Alcohol</u>

<u>3) Alkene</u>

<u>4) Ketone</u>

See figure 2.

I hope it helps!

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Consider the reaction of diboron trioxide with carbon and chlorine. B2O3 (s) + 3C (s) + 3Cl2 (g) 2BCl3 (g) + 3CO (g) Determine t
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In order to identify the limiting reagent calculate the moles of B2O3, C and Cl2. The reagent with the lowest moles is the limiting reactant

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Since the moles of B2O3 < C < Cl2, the limiting reactant is B2O3

Based on the reaction stoichiometry:

1 mole of B2O3 produces 2 moles of BCl3

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8 0
3 years ago
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Irina18 [472]

Empirical formula mass

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Molecular formula

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