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Presented by Leticia Bonita Prince Newcastle University 4 th Year MChem Student.

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Presentation on theme: "Presented by Leticia Bonita Prince Newcastle University 4 th Year MChem Student."— Presentation transcript:

1 Presented by Leticia Bonita Prince Newcastle University 4 th Year MChem Student

2 Aims of Today Increase your understanding of carboxylic acids Increase your spatial skills and awareness using software designed by the CCDC

3 What are Spatial Skills? The ability to mentally manipulate 2-dimensional and 3- dimensional figures. Important in chemistry, biology, medicine, mathematics, physics and everyday life.

4 Carboxylic Acids They have the general formula RCOOH (R= H, CH 3, CH 2 CH 3 etc). Good Hydrogen bond DONORS and ACCEPTORS.

5 Nomenclature Look at the R group and add “-oic acid” to it. If there are two carboxylic acid functional groups, you will add –dioic acid to it.

6 Salts Carboxylic acids are more acid than alcohols because their conjugate base is resonance stabilised. This anion can form a salt by bonding ionically with a metal such as sodium.

7 Boiling Points Carboxylic acids have higher boiling points than alcohols. They dimerise through hydrogen bonding creating a bigger molecule which has larger van der Waals’ – more energy to overcome.

8 Solubility In water, the carboxylic acid will form hydrogen bonds with water instead of dimerising which is why some are soluble. HOWEVER, if there is a large alkyl chain (5 carbons +) the carboxylic won’t dissolve due the hydrophobic nature of the R group.

9 Reactions Esters Alcohols Amides Carboxylate Salts Acyl Chlorides Acid Anhydrides

10 Esterification

11 The WebCSD Type in http://webcsd.ccdc.cam.ac.uk/teaching_database_demo.php http://webcsd.ccdc.cam.ac.uk/teaching_database_demo.php Answer the questions by typing the refcodes into the “find entry” box

12 THANK YOU! ENJOY THE REST OF YOUR DAY!


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