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Flashcards for Hydrocarbons, Alcohols, Phenols, Aldehydes & Ketones, and Carboxylic Acids & Derivatives
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Hydrocarbons
Organic compounds made of carbon and hydrogen atoms.
Acyclic Hydrocarbons
Open-chain hydrocarbons (also known as aliphatic hydrocarbons).
Cyclic Hydrocarbons
Closed-chain hydrocarbons.
Saturated Hydrocarbons
Hydrocarbons containing only single bonds (e.g., alkanes, cycloalkanes).
Unsaturated Hydrocarbons
Hydrocarbons containing double or triple bonds (e.g., alkenes, alkynes, cycloalkenes, cycloalkynes).
Alkanes
Saturated acyclic hydrocarbons.
Alkenes
Unsaturated acyclic hydrocarbons containing at least one double bond.
Alkynes
Unsaturated acyclic hydrocarbons containing at least one triple bond.
Alicyclic Hydrocarbons
Cyclic aliphatic hydrocarbons (saturated or unsaturated).
Aromatic Hydrocarbons
Cyclic hydrocarbons with alternating single and double bonds (e.g., benzene).
Complete Combustion of Hydrocarbons
Reaction of a hydrocarbon with excess oxygen to produce carbon dioxide and water.
Baeyer Test
Test for multiple bonds using potassium permanganate (KMnO4), where the purple solution turns into a brown solid (MnO2) in the presence of alkenes or alkynes.
Substitution Reactions
Reactions that saturated hydrocarbons (alkanes and cycloalkanes) typically undergo under rigorous conditions.
Addition Reactions
Reactions that unsaturated hydrocarbons (alkenes and alkynes) undergo.
Electrophilic Aromatic Substitution
Reactions that aromatic compounds like benzene undergo.
Alcohols
Organic compounds containing one or more hydroxyl (-OH) functional groups attached to a hydrocarbon skeleton. R-OH
Monohydric Alcohol
An alcohol with one hydroxyl (-OH) group (e.g., methanol).
Diol
An alcohol with two hydroxyl (-OH) groups (e.g., ethylene glycol).
Triol
An alcohol with three hydroxyl (-OH) groups (e.g., glycerol).
Primary Alcohol (1°)
An alcohol where the carbon atom bonded to the -OH group is attached to one other carbon atom.
Secondary Alcohol (2°)
An alcohol where the carbon atom bonded to the -OH group is attached to two other carbon atoms.
Tertiary Alcohol (3°)
An alcohol where the carbon atom bonded to the -OH group is attached to three other carbon atoms.
Chromic Acid Test
A test to distinguish primary and secondary alcohols from tertiary alcohols. Positive result: orange to green color change.
Lucas Test
A test to distinguish tertiary and secondary alcohols from primary alcohols using Lucas reagent (HCl and ZnCl2). Positive result: formation of insoluble layer or cloudiness.
Esterification
Reaction between an alcohol and a carboxylic acid to form an ester and water.
Methyl Salicylate
An ester with a wintergreen odor, formed from salicylic acid and methanol.
Iodoform Test
A test for compounds containing the acetyl group (CH3CO-) or secondary alcohols that can be oxidized to form the acetyl group. Positive result: yellow precipitate of CHI3 (iodoform).
Acrolein Test
Test for glycerol. Positive result: Pungent odor.
Fermentation
The conversion of glucose to ethyl alcohol and carbon dioxide by yeast.
Phenol
Aromatic organic compound with a hydroxyl (-OH) group attached to a benzene ring (Ar-OH).
Liquid Phenol
Phenol containing over 50% phenol.
Solubility in Alkali (Phenols)
Phenols react with NaOH to form a colorless solution containing sodium phenoxide.
Reaction with FeCl3 (Phenols)
Phenols give a violet color when treated with dilute FeCl3.
Bromine Water Test (Phenols)
Phenols react with bromine water to form a white precipitate of 2,4,6-tribromophenol.
Phenolphthalein Formation
Formation of phenolphthalein from phenol, which is pink with NaOH and clear with HCl.
Millon's Test
A test for the presence of a phenolic group in tyrosine and proteins containing tyrosine. Positive result: flesh to red precipitate with Millon’s reagent (HgNO3 in HNO3).
Aldehyde
Organic compound containing a carbonyl group (C=O) with at least one hydrogen atom attached to the carbonyl carbon (RCOH).
Ketone
Organic compound containing a carbonyl group (C=O) with two carbon groups attached to the carbonyl carbon (RCOR).
2,4-DNPH (Brady's) Test
Test for carbonyl group (C=O). Positive result: yellow to red precipitate.
Sodium Bisulfite Test
Test for carbonyl group. Positive result: white precipitate.
Schiff's Test
Test for aldehydes. Positive result: violet-colored complex.
Tollen's Test
Test for aldehydes using ammoniacal AgNO3. Positive result: silvery or mirror-like appearance.
Fehling's Test
Test for aldehydes using copper(II) sulfate. Positive result: yellow to brick-red precipitate.
Sodium Nitroprusside Test
Test for methyl ketones. Positive result: bright red to wine red color.
Molisch Test
General test for carbohydrates. Positive result: violet layer or ring.
Bial's Orcinol Test
Test to differentiate hexoses from pentoses using orcinol, HCl, and ferric chloride. Hexoses give brown, pentoses give blue to green.
Carboxylic Acids
Organic compounds containing a carboxy group (-COOH).
Ester
A carboxylic acid derivative with the structure R-C(=O)-OR'.
Amide
A carboxylic acid derivative with the structure R-C(=O)-NR'R''.
Acyl Chloride
A carboxylic acid derivative with the structure R-C(=O)-Cl.
Acid Anhydride
A carboxylic acid derivative with the structure (R-C(=O))-O-(C(=O)-R).
Reaction with Water and Indicators (Carboxylic Acids)
Carboxylic acids react with water to form carboxylate and hydronium ions, changing litmus paper to red.
Reaction with NaOH (Carboxylic Acids)
Carboxylic acids react with sodium hydroxide to form a salt and water.
Reaction with Na2CO3 (Carboxylic Acids)
Carboxylic acids react with sodium carbonate to release CO2 gas, differentiating them from weaker acids like alcohols and phenols.
Reaction with Neutral FeCl3 (Carboxylic Acids)
Acetic acid forms a red-orange solution with reddish-brown precipitate; tartaric acid forms a soluble yellow solution.
Hydroxamic Test
Test for esters. Positive result: magenta or burgundy color after adding ferric chloride.
Saponification
alkaline hydrolysis of fats and oils (triglycerides) which produces a salt of fatty acids called soap and glycerol.