1) Draw a carboxylic acid between 7-9 carbons. Give the IUPAC name. 2) React this carboxylic acid with NaOH (neutralization reaction). Write out the reaction and product formed. Write the name of the salt formed. 3) What is the solubility of the carboxylic acid and what is the solubility of the product carboxylate salt formed. Explain.

Chemistry for Today: General, Organic, and Biochemistry
9th Edition
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Chapter15: Carboxylic Acids And Esters
Section: Chapter Questions
Problem 15.64E
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i’m practicing some old textbook pages for a midterm could someone help me with these
1) Draw a carboxylic acid between 7-9 carbons. Give the IUPAC name.
2) React this carboxylic acid with NaOH (neutralization reaction). Write out the
reaction and product formed. Write the name of the salt formed.
3) What is the solubility of the carboxylic acid and what is the solubility of the
product carboxylate salt formed. Explain.
4) React your carboxylic acid with ethanol using an acid catalyst and heat
(esterification). Give the name of the ester formed.
5) Give the IUPAC name of the carboxylic acid and alcohol used to make propyl
butanoate, an ester. Hint: Draw the ester first and work your way backwards to the
original carboxylic acid and alcohol need to produce propyl butanoate.
Transcribed Image Text:1) Draw a carboxylic acid between 7-9 carbons. Give the IUPAC name. 2) React this carboxylic acid with NaOH (neutralization reaction). Write out the reaction and product formed. Write the name of the salt formed. 3) What is the solubility of the carboxylic acid and what is the solubility of the product carboxylate salt formed. Explain. 4) React your carboxylic acid with ethanol using an acid catalyst and heat (esterification). Give the name of the ester formed. 5) Give the IUPAC name of the carboxylic acid and alcohol used to make propyl butanoate, an ester. Hint: Draw the ester first and work your way backwards to the original carboxylic acid and alcohol need to produce propyl butanoate.
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