Yes, at approx 182 K.
cyclobutane
radical reaction of chlorine with cyclobutane yields chlorocyclobutane and hydrogen chloride
Yes, cyclobutane is more reactive than butane due to its ring strain caused by the angle strain in the cyclobutane ring. This strain makes cyclobutane more prone to ring-opening reactions compared to butane.
Cyclobutane is used in organic chemistry as a building block to synthesize other compounds. It is also used in the understanding of strain in small cyclic molecules and in theoretical studies of ring strain. Additionally, cyclobutane derivatives have been investigated for potential medicinal applications.
The boiling point of cyclobutane is approximately 49°C (120°F) at standard atmospheric pressure.
No, butane is not a constitutional isomer of cyclobutane. Butane is a straight-chain alkane with four carbon atoms in a row, while cyclobutane is a cyclic compound with four carbon atoms forming a ring. Constitutional isomers have the same molecular formula but different connectivity of atoms.
6
Cyclopropane Cyclobutane Cyclopentane Cyclohexane Cycloheptane Cycloalkane
There 4 isomers : 1) H2C=CHCH2CH3 => but-1-ene 2) CH3CH=CHCH3 => but-2-ene 3) (CH3)2C=CHCH3 => 2- methylpropene 4) CH2-CH2-CH2-CH2 => cyclobutane/cycloalkane. C4h8 has 3 isomers from the same homologous series and one that is not from the same homologous series.
Empirical formula (lowest whole number) for C4H8 is CH2, obtained by dividing by 4.
There are more than 20 stuctural isomers of hexene C6H12, including various branched (cis and trans) and cyclic compounds (eg. cyclohexane, methyl-cylopentane, 1,1-dimethyl-cyclobutane, 1,2-dimethyl-cyclobutane, 1,3-dimethyl-cyclobutane, and some other, maybe not stable, propyl/methyl-ethyl/trimethyl-cyclopropanes) Some of them also count for optical isomerism (eg. 3*-methyl-1-pentene)
Yes it can freeze.