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47 Cards in this Set

  • Front
  • Back

Formic Acid

Ant bite

Acetic Acid

Vinegae

Propionic Acid

Swiss Cheese

Butyric Acid

Rancid butter

Valeric Acid

Valerian root

Caproic Acid

Goat fat (hexanoic)

Caprylic Acid

Goat fat (octanoic)

Capric Acid

Goat fat (decanoic)

Palmitic Acid

Palm oil

Stearic Acid

Beef fat = tallow (octadecanoic)

Heptanoic (ethanic) Acid

Odor of rancid oil

Octanoic (caprylic) Acid

Hunger-stimukating effect on the hypothalamus

Triglycerides

Major energy storage in many animals and plants


Saturated = solid fat


Unsaturated = liquid fat


Kidney stones

Calcium salt of oxalic acid

Malonic Acid

Synthesis of barbiturates

Succinic Acid

Intermediates of the citric acid cycle (amber)

Glutamic acid

Production of condensation polymers

Adipic acid

Tartness to soft drinks and helps slow down food spoilage.


Also for the synthesis of nylon, polyurethane and plasticizers.

Citric Acid

Sharp taste to sour candies, citrus fruits, preservatives and antioxidant.

Lactic acid

Product of fermentation of sugars

Tartaric acid

Baking powder

Malic acid

Green apples

Sodium salt of benzoic acid

Preservative

Salicylic acid

Disinfectant

Acetylsalicylic acid

Aspirin - willow bark

Terepthalic acid

Synthesize PETE

Ethyl butanoate

Pineapple

Propyl ethanoate

Pears

Isobutyl methanoate

Rasberries

3-Methylbutyl ethanoate

Bananas

Octyl ethanoate

Oranges

Methyl butanoate

Apples

Pentyl butanoate

Apricots

Methyl thiobutanoate

Strawberries

Preparation of Carboxylic Acids

Acid - Base Reaction

Fischer Esterification

Esters

Slightly polar


Pleasant aromas


-OH is replaced with -OR


Boil at sound same temperature as Aldehydes and Ketones


Simpler ones are somewhat soluble in water


Cyclic esters =lactone

Preparation of Esters

Fischer Esterification

Hydrolysis of Esters

Addition of a water molecule


Reverse of Esterification

Base - catalyzed Hydrolysis (Saponification)

Acid chlorides

Acid Chlorides

Slightly polar Boil at around the same temperature as an aldehyde or ketone


React violently with water


Activated form of Carboxylic acid

Acid Anhydrides

Acid Anhydrides

Without water


Readily undergo hydrolysis and the product is a Carboxylic acid


Can react with alcohol and form an Ester and Carboxylic acid

Acid Anhydrides

Phosphoesters and Thioesters