Difference between revisions of "Functional group"

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A '''functional group''' is any one of a number of specific combinations of [[molecule]]s within an [[atom]]. Used mainly in [[organic chemistry]], functional groups are a helpful way to determine the structure and function of a molecule, as functional groups act very similar no matter what molecule they are a part of <ref name="mcmurry">McMurry, John. Organic Chemistry, 6e. Brooks/Cole: 2004.</ref>.
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A '''functional group''' is any one of a number of specific combinations of [[molecule]]s within an [[atom]]. Used mainly in [[organic chemistry]], functional groups are a helpful way to determine the structure and function of a molecule, as functional groups act very similar no matter what molecule they are a part of.<ref name="mcmurry">McMurry, John. Organic Chemistry, 6e. Brooks/Cole: 2004.</ref>
  
 
A generic functional group is represented by the letter R in a [[chemical formula]]. For instance, CR<sub>4</sub> represents a carbon with four of the same functional group bonded to it.
 
A generic functional group is represented by the letter R in a [[chemical formula]]. For instance, CR<sub>4</sub> represents a carbon with four of the same functional group bonded to it.
  
Some functional groups are described in the following table: <ref name="mcmurry" />
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Some functional groups are described in the following table:<ref name="mcmurry" />
  
 
{|class="wikitable" style="text-align:left"
 
{|class="wikitable" style="text-align:left"
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|[[Aromatic ring|Arene]] || Unsaturated six-carbon ring || none || Benzene (C<sub>6</sub>H<sub>6</sub>)
 
|[[Aromatic ring|Arene]] || Unsaturated six-carbon ring || none || Benzene (C<sub>6</sub>H<sub>6</sub>)
 
|-
 
|-
|[[Halide]] || [[Covalent bond|covalantly bonded]] [[fluorine|F]], [[chlorine|Cl]], [[bromine|Br]] or [[iodine|I]] || none || Chloroethane (ClCH<sub>2</sub>CH<sub>3</sub>
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|[[Halide]] || [[Covalent bond|covalantly bonded]] [[fluorine|F]], [[chlorine|Cl]], [[bromine|Br]] or [[iodine|I]] || none || Chloroethane (ClCH<sub>2</sub>CH<sub>3</sub>)
 
|-
 
|-
 
|[[Alcohol]] || Covalantly bonded -OH || -''ol'' || Ethanol (CH<sub>3</sub>CH<sub>2</sub>OH)
 
|[[Alcohol]] || Covalantly bonded -OH || -''ol'' || Ethanol (CH<sub>3</sub>CH<sub>2</sub>OH)
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|[[Ketone]] || Double bonded O || -''one'' || Methyl ethyl ketone (CH<sub>3</sub>(CO)C<sub>2</sub>H<sub>5</sub>)
 
|[[Ketone]] || Double bonded O || -''one'' || Methyl ethyl ketone (CH<sub>3</sub>(CO)C<sub>2</sub>H<sub>5</sub>)
 
|-
 
|-
|[[Aldehyde]] || Double bonded O attached to a carbon attached to a hydrogen|| -''al'' || Acetaldehyde (C<sub>2</sub>H<sub>4</sub>O)
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|[[Aldehyde]] || Double bonded O attached to a carbon attached to a hydrogen|| -''al'' || [[Acetaldehyde]] (C<sub>2</sub>H<sub>4</sub>O)
 
|-
 
|-
 
|[[Ether]] || Oxygen bonded to two other carbons || ''ether'' || Diethyl ether (CH<sub>3</sub>CH<sub>2</sub>OCH<sub>2</sub>CH<sub>3</sub>
 
|[[Ether]] || Oxygen bonded to two other carbons || ''ether'' || Diethyl ether (CH<sub>3</sub>CH<sub>2</sub>OCH<sub>2</sub>CH<sub>3</sub>
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|-
 
|-
 
|[[Carboxylic acid]] || Carbon double bonded to O and bonded to -OH || -''oic acid'' || [[Acetic acid|Ethanoic acid]] (CH<sub>3</sub>COOH)
 
|[[Carboxylic acid]] || Carbon double bonded to O and bonded to -OH || -''oic acid'' || [[Acetic acid|Ethanoic acid]] (CH<sub>3</sub>COOH)
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|-
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|Carbonyl<ref>[https://chem.libretexts.org/?title=Core/Organic_Chemistry/Aldehydes_and_Ketones/Properties_of_Aldehydes_%26_Ketones/The_Carbonyl_Group The Carbonyl Group]</ref> || Carbon double bonded to Oxygen, C=O || - || Forms part of many larger functional groups
 
|}
 
|}
  

Latest revision as of 21:42, March 15, 2017

A functional group is any one of a number of specific combinations of molecules within an atom. Used mainly in organic chemistry, functional groups are a helpful way to determine the structure and function of a molecule, as functional groups act very similar no matter what molecule they are a part of.[1]

A generic functional group is represented by the letter R in a chemical formula. For instance, CR4 represents a carbon with four of the same functional group bonded to it.

Some functional groups are described in the following table:[1]

Name Description Ending Simple Example
Alkane Carbon-carbon single bond -ane Ethane (CH3CH3)
Alkene Carbon-carbon double bond -ene Ethene (CH2CH2)
Alkyne Carbon-carbon triple bond -yne Ethyne (CHCH)
Arene Unsaturated six-carbon ring none Benzene (C6H6)
Halide covalantly bonded F, Cl, Br or I none Chloroethane (ClCH2CH3)
Alcohol Covalantly bonded -OH -ol Ethanol (CH3CH2OH)
Ketone Double bonded O -one Methyl ethyl ketone (CH3(CO)C2H5)
Aldehyde Double bonded O attached to a carbon attached to a hydrogen -al Acetaldehyde (C2H4O)
Ether Oxygen bonded to two other carbons ether Diethyl ether (CH3CH2OCH2CH3
Ester Oxygen double bonded to a carbon which is also bonded to another oxygen ester Diethyl ester (CH3CH2OOCHCH3
Amine -NR2 -amine Ethylamine (CH3CH2NH2)
Amide Double bonded O attached to a carbon attached to a nitrogen -amide Ethanamide (CH3CONH2)
Carboxylic acid Carbon double bonded to O and bonded to -OH -oic acid Ethanoic acid (CH3COOH)
Carbonyl[2] Carbon double bonded to Oxygen, C=O - Forms part of many larger functional groups

References

  1. ↑ 1.0 1.1 McMurry, John. Organic Chemistry, 6e. Brooks/Cole: 2004.
  2. ↑ The Carbonyl Group