What is the structure of a compound with the formula C7H14O that has an ether and cyclobutane ring, including its IUPAC name? In addition, what is the structure of the compound with the formula C7H14O that does NOT contain the functional groups: epoxide, ether, cycloalkane, alcohol, alkene. Indicate the functional groups used that are present in the structure made for this compound.

Structural formula of 2-ethyl-3-methylheptanol

please give iupac name and Classify the following compounds as to what organic group it belongs. Choices: alkane, alkene, alkyne, arene, alcohol, phenol, ether, aldehyde, ketone, thiol.If it is an alcohol indicate the type/classification.

1,3-Propanediol, HOCH₂CH₂CH₂OH, is a diol used as a building block in the production of polymers for use in adhesives and coatings. Draw the condensed structure of the most oxidized product formed after the oxidation of 1,3-propanediol.

Alkenes can be converted to alcohols by reaction with mercuric acetate to form a β-hydroxyalkylmercury(II) acetate compound, a reaction called oxymercuration. Subsequent reduction with NaBH4 reduces the C–Hg bond to a C–H bond, forming the alkyl alcohol, a reaction called demercuration. Draw the structures of the Hg-containing compound(s) and the final alcohol product(s) formed in the following reaction sequence, omitting byproducts. If applicable, draw hydrogen at a chirality center and indicate stereochemistry via wedge-and-dash bonds.

What alcohol is formed by the addition of water in the presence of sulfuric acid (an addition reaction) to 1-pentene?

Alkenes can be converted to alcohols by reaction with mercuric acetate to form a β-hydroxyalkylmercury(II) acetate compound, a reaction called oxymercuration. Subsequent reduction with NaBH4 reduces the C–Hg bond to a C–H bond, forming the alkyl alcohol, a reaction called demercuration. Draw the structures of the Hg-containing compound(s) and the final alcohol product(s) formed in the following reaction sequence, omitting byproducts. If applicable, draw hydrogen at a chirality center and indicate stereochemistry via wedge-and-dash bonds.

What is the difference between a saturated hydrocarbon and an unsaturated hydrocarbon? Unsaturated hydrocarbons have no multiple covalent bonds. The unsaturated hydrocarbon has at least one multiple covalent bond. Unsaturated hydrocarbons must not have cis/trans isomers O Unsaturated hydrocarbons must have at least two atoms joined by bonds that can rotate