orgo 1: functional groups

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30 Terms

1
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alkane

hydrocarbon backbone

all single bonds

“saturated”

2
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alkene

hydrocarbon backbone

at least 1 double bond

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alkyne

hydrocarbon backbone

at least 1 triple bond

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aromatic

ring structure

very stable

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why are functional groups important?

site of chemical reactivity, intermolecular forces

contribute to chemical and physical properties

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aliphatic definition

non-ring structure (chain of carbon)

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haloalkane/alkylhalide

carbon chain with any halogen

RX

<p>carbon chain with any halogen</p><p>RX</p>
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haloalkane/alkylhalide naming

halogen name + named carbon chain

<p>halogen name + named carbon chain</p>
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alcohol

attached hydroxyl group

ROH

<p>attached hydroxyl group</p><p>ROH</p>
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alcohol naming

carbon chain/attached name + “ol”

<p>carbon chain/attached name + “ol”</p>
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ether

oxygen within backbone

ROR

<p>oxygen within backbone</p><p>ROR</p>
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ether naming

chain before carbon name + “oxy” + chain after carbon name

or

carbon chain names + ether (dimethyl ether)

<p>chain before carbon name + “oxy” + chain after carbon name</p><p>or</p><p>carbon chain names + ether (dimethyl ether)</p>
13
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amine

nitrogen in carbon chain

RNH2, R2NH, R3N

<p>nitrogen in carbon chain</p><p>RNH2, R2NH, R3N</p>
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amine naming

carbon chain name + amine

<p>carbon chain name + amine</p>
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carbonyl functional group defining feature

oxygen double bonded to C of backbone

<p>oxygen double bonded to C of backbone</p>
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aldehyde

carbonyl with hydrogen & R group

RC(O)H

<p>carbonyl with hydrogen &amp; R group</p><p>RC(O)H</p>
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aldehyde naming

carbon chain + “al”

or

carbon chain name + “aldehyde”

<p>carbon chain + “al”</p><p>or</p><p>carbon chain name + “aldehyde”</p>
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ketone

carbon chain on either side of carbonyl

RC(O)R’

<p>carbon chain on either side of carbonyl</p><p>RC(O)R’</p>
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ketone naming

carbon (parent) chain name + “one”

<p>carbon (parent) chain name + “one”</p>
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carboxylic acid

hydroxyl group attached directly to carbonyl

RC(O)OH

<p>hydroxyl group attached directly to carbonyl</p><p>RC(O)OH</p>
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carboxylic acid naming

carbon chain name + “-ic acid”

<p>carbon chain name + “-ic acid”</p>
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ester

carbonyl attached to oxygen within the backbone

RC(O)OR’

<p>carbonyl attached to oxygen within the backbone</p><p>RC(O)OR’</p>
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ester naming

first carbon chain name + second carbon chain name + “ate”

<p>first carbon chain name + second carbon chain name + “ate”</p>
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amide

carbonyl attached to nitrogen within backbone

RC(O)NH2, RC(O)NHR’, …

<p>carbonyl attached to nitrogen within backbone</p><p>RC(O)NH2, RC(O)NHR’, …</p>
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amide naming

name carbon chain + “amide”

<p>name carbon chain + “amide”</p>
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nitrile

carbon & nitrogen triple bonded

cyanide alternative name

RCN

<p>carbon &amp; nitrogen triple bonded</p><p>cyanide alternative name</p><p>RCN</p>
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nitrile naming

name of carbon chain + “nitrile”

<p>name of carbon chain + “nitrile”</p>
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alkylhalides/haloalkynes classification

classified by how many C’s/H’s the C attached to the halogen is bound to

halogen - C - C’s & H’s classified by

1o — 2 H, 1 C

2o — 1 H, 2 C

3o — 0 H, 3 C

<p>classified by how many C’s/H’s the C attached to the halogen is bound to</p><p></p><p>halogen - C - C’s &amp; H’s classified by</p><p></p><p>1<sup>o </sup>— 2 H, 1 C</p><p>2<sup>o</sup> — 1 H, 2 C</p><p>3<sup>o</sup> — 0 H, 3 C</p>
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alcohol classification

classified by how many C’s/H’s the C attached to the hydroxide is bound to

hydroxide - C - C’s & H’s classified by

1o — 2 H, 1 C

2o — 1 H, 2 C

3o — 0 H, 3 C

<p>classified by how many C’s/H’s the C attached to the hydroxide is bound to</p><p></p><p>hydroxide - C - C’s &amp; H’s classified by</p><p></p><p>1<sup>o </sup>— 2 H, 1 C</p><p>2<sup>o</sup> — 1 H, 2 C</p><p>3<sup>o</sup> — 0 H, 3 C</p>
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amine classification

named by how many groups (NOT H) are attached to N

0o — NH3 (ammonia)

1o — NRH2

2o — NR2H2

3o — NR3

<p>named by how many groups (NOT H) are attached to N</p><p></p><p>0<sup>o</sup> — NH3 (ammonia)</p><p>1<sup>o </sup>— NRH2</p><p>2<sup>o</sup> — NR2H2</p><p>3<sup>o</sup> — NR3</p>