chemistry organic compounds

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17 Terms

1
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<p>What defines a <strong>Saturated Hydrocarbon</strong>?</p>

What defines a Saturated Hydrocarbon?

A hydrocarbon containing only single bonds between carbon atoms. It follows the general formula CnH2n+2.

2
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<p>What are the general formula and typical suffix for <strong>Alkanes</strong>?</p>

What are the general formula and typical suffix for Alkanes?

  • General Formula: CnH2n+2. Suffix: -ane. (e.g., methane, ethane, propane, butane)

3
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<p>What are the general formula and typical suffix for <strong>Alkenes</strong>?</p>

What are the general formula and typical suffix for Alkenes?

CnH2n. Suffix: -ene. (Contains at least one carbon-carbon double bond)

4
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<p>What are the general formula and typical suffix for <strong>Alkynes</strong>?</p>

What are the general formula and typical suffix for Alkynes?

General Formula: CnH2n-2. Suffix: -yne. (Contains at least one carbon-carbon triple bond)

5
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<p>Define <strong>Alkyl Group</strong> and give common examples.</p>

Define Alkyl Group and give common examples.

A functional group consisting of an alkane chain missing one hydrogen atom. Examples: methyl (-CH3), ethyl (-CH2CH3), propyl (-CH2CH2CH3), butyl (-CH2CH2CH2CH3).

6
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<p>Define <strong>Isomers</strong> in organic chemistry.</p>

Define Isomers in organic chemistry.

Compounds with the same molecular formula but different structural formulas (different arrangement of atoms).

7
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<p>What are <strong>Structural Isomers</strong>?</p>

What are Structural Isomers?

Isomers that differ in the connectivity of their atoms (e.g., n-butane vs. isobutane).

8
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<p>What are <strong>Functional Group Isomers</strong>?</p>

What are Functional Group Isomers?

Isomers that have the same molecular formula but different functional groups (e.g., ethanol (an alcohol) vs. dimethyl ether (an ether), both C2H6O).

9
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List typical characteristics of most Organic Compounds.

Low boiling/melting points, generally poor conductors of electricity, often insoluble in water (nonpolar).

10
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<p>What is the functional group and suffix for <strong>Alcohols</strong>?</p>

What is the functional group and suffix for Alcohols?

Functional Group: Hydroxyl group (-OH). Suffix: -ol.

11
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<p>What is the functional group and suffix for <strong>Carboxylic Acids</strong>?</p>

What is the functional group and suffix for Carboxylic Acids?

  • Functional Group: Carboxyl group (-COOH or -C(=O)OH). Suffix: -oic acid.

12
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<p>What is the functional group and suffix for <strong>Amides</strong>?</p>

What is the functional group and suffix for Amides?

Functional Group: Amide group (-CONH2 or -C(=O)NH2). Suffix: -amide.

13
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<p>What is the functional group and typical suffix for <strong>Amines</strong>?</p>

What is the functional group and typical suffix for Amines?

  • Functional Group: Amine group (-NH2, -NHR, -NR2). Suffix: -amine (or treated as a substituent using amino-).

14
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<ul><li><p>How are <strong>Halogenated Hydrocarbons</strong> typically named?</p></li><li><p></p></li></ul><p></p>
  • How are Halogenated Hydrocarbons typically named?

  • By using prefixes for the halogen atoms (e.g., chloro- for chlorine, bromo- for bromine, fluoro- for fluorine, iodo- for iodine) before the parent alkane name, with numbers indicating position.

15
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<p>Describe an <strong>Addition Reaction</strong> in organic chemistry.</p>

Describe an Addition Reaction in organic chemistry.

  • A reaction where atoms are added to an unsaturated molecule (containing double or triple bonds), breaking the multiple bond and forming new single bonds. (e.g., alkene + halogen)

16
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<p>Describe a <strong>Substitution Reaction</strong> in organic chemistry.</p>

Describe a Substitution Reaction in organic chemistry.

A reaction where an atom or group of atoms in a molecule is replaced by another atom or group of atoms. (e.g., alkane + halogen)

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<p>What is a <strong>Halogenated Hydrocarbon</strong>?</p>

What is a Halogenated Hydrocarbon?

An organic compound where one or more hydrogen atoms of a hydrocarbon have been replaced by one or more halogen atoms (F, Cl, Br, I).

  • Example: Chloromethane (CH3Cl), 1,2-Dichloroethane (CH2Cl-CH2Cl)