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Crotyl groups attached to R. A crotyl group is an organic functional group with the formula RCH 2 CH=CHCH 3. [1] Systematically, it is called a but-2-en-1-yl group and exhibits geometric isomerism, being either cis (Z) or trans (E).
Butenoic acid is any of three monocarboxylic acids with an unbranched 4-carbon chain with 3 single bonds and one double bond; that is, with the structural formula HO(O=)C – CH=CH – CH 2 –H (2-butenoic) or HO(O=)C – CH 2 – CH=CH –H (3-butenoic). All have the chemical formula C 3 H 5 COOH or C 4 H 6 O 2. These compounds are ...
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Structural formula nonanoic acid: pelargonic acid 1-octanecarboxylic acid: CH 3 (CH 2) 7 COOH benzene-1,3,5-tricarboxylic acid: trimesic acid: C 6 H 3 (COOH) 3 (E)-3-phenylprop-2-enoic acid: cinnamic acid trans-cinnamic acid phenylacrylic acid cinnamylic acid 3-phenylacrylic acid (E)-cinnamic acid benzenepropenoic acid isocinnamic acid: C 6 H 5 ...
But-2-ene is an acyclic alkene with four carbon atoms. It is the simplest alkene exhibiting cis/trans-isomerism (also known as (E/Z)-isomerism); that is, it exists as two geometric isomers cis-but-2-ene ((Z)-but-2-ene) and trans-but-2-ene ((E)-but-2-ene). It is a petrochemical, produced by the catalytic cracking of crude oil or the dimerization ...
Butanol (also called butyl alcohol) is a four-carbon alcohol with a formula of C 4 H 9 O H, which occurs in five isomeric structures (four structural isomers), from a straight-chain primary alcohol to a branched-chain tertiary alcohol; [1] all are a butyl or isobutyl group linked to a hydroxyl group (sometimes represented as BuOH, sec-BuOH, i-BuOH, and t-BuOH).
C 4 H 6 O 2: crotonic acid: 3724-65-0 C 4 H 6 O 2: diacetyl: C 4 H 6 O 2: diepoxybutane: C 4 H 6 O 2: 1,4-Dioxene: C 4 H 6 O 2: isocrotonic acid: C 4 H 6 O 2: methacrylic acid: 79-41-4 C 4 H 6 O 2: methyl acrylate: C 4 H 6 O 2: succinaldehyde: C 4 H 6 O 2: vinyl acetate: C 4 H 6 O 3: propylene carbonate: C 4 H 6 O 4: succinic acid: 110-15-6 C 4 ...
Another example of this is the relationship between oleic acid and elaidic acid; oleic acid, the cis isomer, has a melting point of 13.4 °C, making it a liquid at room temperature, while the trans isomer, elaidic acid, has the much higher melting point of 43 °C, due to the straighter trans isomer being able to pack more tightly, and is solid ...