Draw the structure of 3,4−dimethyl−3−heptanol. Draw the structure of n−heptane and selectively replace hydrogens with two methyl groups and one ―OH group

16. An atom or group of atoms that can give organic compounds distinct chemical and physical properties. 21. When a compound with the general formula R-COOH loses a proton, the product that remains is described with this term.  Its general formula is R-COO- 24. A class of organic compounds in which three or more carbons form a ring structure.  All of the carbon-to-carbon bonds are single bonds in this family of compounds.

Draw the skeletal ("line") structure of the organic molecule that produces sodium 2,3-dihydroxybutanoate when reacted with NaOH. c* Click and drag to start drawing a structure.

Please help me draw these organic structures properly. 1. Tert-butyl bromide 2. 3,4-dibromohex-1-ene 3. 3-ethyl-2-nitropentanoic acid

What are the hybridization and bond angles of the oxygens in benzoic acid?

Ketone   Amine   Ester   Carboxylic Acid   Amide   Nitrile   Peroxide   Alkyne   Thiol

Aldehyde,carboxylic acid,ketone,no product

Do not give handwriting solution.

2.a What is the molar mass of acetylsalicylic acid (aspirin)? b. Name the functional groups on the hydrocarbon ring present in acetylsalicylic acid. Circle them below. H H H H OH H -C-C-H OH

Explain why these compounds (1-propanol, ethylene glycol, and ethanethiol) experience different intermolecular forces based on their molecular structure.