Home Chemistry Organic Building Blocks Aliphatic Cyclic Hydrocarbons Cycloheptane
Combustion: Cycloheptane can burn in the presence of oxygen to produce carbon dioxide and water. The combustion reaction is exothermic and releases energy.
Halogenation: Cycloheptane can undergo halogenation reactions, where hydrogen atoms in the ring are replaced by halogen atoms (e.g., chlorine or bromine) in the presence of a halogenating agent like chlorine gas or bromine gas.
Hydrogenation: In the presence of a catalyst like platinum or palladium, cycloheptane can be hydrogenated to form cycloheptane, where double bonds are converted into single bonds by the addition of hydrogen atoms.
Oxidation: Cycloheptane can be oxidized by strong oxidizing agents to produce various products, depending on the reaction conditions. For example, it can be oxidized to cycloheptanol or cycloheptanone.
Ring Opening: Under certain reaction conditions, cycloheptane can undergo ring-opening reactions to form open-chain compounds. This often requires high temperatures and specific catalysts.
Substitution Reactions: Similar to other cycloalkanes, cycloheptane can undergo substitution reactions where one or more hydrogen atoms are replaced by other functional groups. This can be achieved through various substitution reactions like halogenation, alkylation, or acylation.
Isomerization: Cycloheptane can undergo isomerization reactions, where the positions of carbon-carbon bonds within the ring can change, resulting in different isomeric forms.
Cycloaddition Reactions: Cycloheptane can participate in cycloaddition reactions with appropriate reactants, leading to the formation of new cyclic compounds.
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(S)-2-((tert-Butoxycarbonyl)amino)-2-cycloheptylacetic acid
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N-Methylcycloheptanamine hydrochloride
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