Organic Chemistry Flashcards

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Flashcards for Hydrocarbons, Alcohols, Phenols, Aldehydes & Ketones, and Carboxylic Acids & Derivatives

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57 Terms

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Hydrocarbons

Organic compounds made of carbon and hydrogen atoms.

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Acyclic Hydrocarbons

Open-chain hydrocarbons (also known as aliphatic hydrocarbons).

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Cyclic Hydrocarbons

Closed-chain hydrocarbons.

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Saturated Hydrocarbons

Hydrocarbons containing only single bonds (e.g., alkanes, cycloalkanes).

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Unsaturated Hydrocarbons

Hydrocarbons containing double or triple bonds (e.g., alkenes, alkynes, cycloalkenes, cycloalkynes).

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Alkanes

Saturated acyclic hydrocarbons.

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Alkenes

Unsaturated acyclic hydrocarbons containing at least one double bond.

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Alkynes

Unsaturated acyclic hydrocarbons containing at least one triple bond.

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Alicyclic Hydrocarbons

Cyclic aliphatic hydrocarbons (saturated or unsaturated).

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Aromatic Hydrocarbons

Cyclic hydrocarbons with alternating single and double bonds (e.g., benzene).

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Complete Combustion of Hydrocarbons

Reaction of a hydrocarbon with excess oxygen to produce carbon dioxide and water.

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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.

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Substitution Reactions

Reactions that saturated hydrocarbons (alkanes and cycloalkanes) typically undergo under rigorous conditions.

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Addition Reactions

Reactions that unsaturated hydrocarbons (alkenes and alkynes) undergo.

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Electrophilic Aromatic Substitution

Reactions that aromatic compounds like benzene undergo.

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Alcohols

Organic compounds containing one or more hydroxyl (-OH) functional groups attached to a hydrocarbon skeleton. R-OH

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Monohydric Alcohol

An alcohol with one hydroxyl (-OH) group (e.g., methanol).

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Diol

An alcohol with two hydroxyl (-OH) groups (e.g., ethylene glycol).

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Triol

An alcohol with three hydroxyl (-OH) groups (e.g., glycerol).

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Primary Alcohol (1°)

An alcohol where the carbon atom bonded to the -OH group is attached to one other carbon atom.

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Secondary Alcohol (2°)

An alcohol where the carbon atom bonded to the -OH group is attached to two other carbon atoms.

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Tertiary Alcohol (3°)

An alcohol where the carbon atom bonded to the -OH group is attached to three other carbon atoms.

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Chromic Acid Test

A test to distinguish primary and secondary alcohols from tertiary alcohols. Positive result: orange to green color change.

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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.

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Esterification

Reaction between an alcohol and a carboxylic acid to form an ester and water.

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Methyl Salicylate

An ester with a wintergreen odor, formed from salicylic acid and methanol.

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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).

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Acrolein Test

Test for glycerol. Positive result: Pungent odor.

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Fermentation

The conversion of glucose to ethyl alcohol and carbon dioxide by yeast.

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Phenol

Aromatic organic compound with a hydroxyl (-OH) group attached to a benzene ring (Ar-OH).

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Liquid Phenol

Phenol containing over 50% phenol.

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Solubility in Alkali (Phenols)

Phenols react with NaOH to form a colorless solution containing sodium phenoxide.

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Reaction with FeCl3 (Phenols)

Phenols give a violet color when treated with dilute FeCl3.

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Bromine Water Test (Phenols)

Phenols react with bromine water to form a white precipitate of 2,4,6-tribromophenol.

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Phenolphthalein Formation

Formation of phenolphthalein from phenol, which is pink with NaOH and clear with HCl.

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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).

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Aldehyde

Organic compound containing a carbonyl group (C=O) with at least one hydrogen atom attached to the carbonyl carbon (RCOH).

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Ketone

Organic compound containing a carbonyl group (C=O) with two carbon groups attached to the carbonyl carbon (RCOR).

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2,4-DNPH (Brady's) Test

Test for carbonyl group (C=O). Positive result: yellow to red precipitate.

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Sodium Bisulfite Test

Test for carbonyl group. Positive result: white precipitate.

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Schiff's Test

Test for aldehydes. Positive result: violet-colored complex.

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Tollen's Test

Test for aldehydes using ammoniacal AgNO3. Positive result: silvery or mirror-like appearance.

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Fehling's Test

Test for aldehydes using copper(II) sulfate. Positive result: yellow to brick-red precipitate.

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Sodium Nitroprusside Test

Test for methyl ketones. Positive result: bright red to wine red color.

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Molisch Test

General test for carbohydrates. Positive result: violet layer or ring.

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Bial's Orcinol Test

Test to differentiate hexoses from pentoses using orcinol, HCl, and ferric chloride. Hexoses give brown, pentoses give blue to green.

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Carboxylic Acids

Organic compounds containing a carboxy group (-COOH).

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Ester

A carboxylic acid derivative with the structure R-C(=O)-OR'.

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Amide

A carboxylic acid derivative with the structure R-C(=O)-NR'R''.

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Acyl Chloride

A carboxylic acid derivative with the structure R-C(=O)-Cl.

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Acid Anhydride

A carboxylic acid derivative with the structure (R-C(=O))-O-(C(=O)-R).

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Reaction with Water and Indicators (Carboxylic Acids)

Carboxylic acids react with water to form carboxylate and hydronium ions, changing litmus paper to red.

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Reaction with NaOH (Carboxylic Acids)

Carboxylic acids react with sodium hydroxide to form a salt and water.

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Reaction with Na2CO3 (Carboxylic Acids)

Carboxylic acids react with sodium carbonate to release CO2 gas, differentiating them from weaker acids like alcohols and phenols.

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Reaction with Neutral FeCl3 (Carboxylic Acids)

Acetic acid forms a red-orange solution with reddish-brown precipitate; tartaric acid forms a soluble yellow solution.

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Hydroxamic Test

Test for esters. Positive result: magenta or burgundy color after adding ferric chloride.

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Saponification

alkaline hydrolysis of fats and oils (triglycerides) which produces a salt of fatty acids called soap and glycerol.