Explain how the acidities of alcohols and thiols is reflected by the element effect

List below three characteristics that a good solvent must satisfy to recrystallize an organic compound that exists in a solid state at room temperature, example: benzoic acid.

One choose the most appropriate name for the following organic molecule. Hexanone, heptanoic acid, hexanoic acid, hexanol, heptanone, or hexanal.

Explain the following concept Why methanol is more soluble in water than propanol?

Discuss what is meant by the term ether and epoxide with respect to organic compounds. Include in your discussion the nomenclature, properties and structure of compounds identified as ethers and epoxide

Explain the intermolecular forces between water and cyclohexane?

What is the functional group of propanoic acid? How do we know if it's soluble in water or not using the flowchart that is attached. which test should be performed using the flowchart. Is propanoic acid a ketone, aldehyde, ester or alcohol and how did you know?what would be the most efficient series of solubility and functional group tests that would identify the functional group? Also what could be the sources of error in this experiment? What could occur that would give false positives, false negatives, or incorrect interpretations?

B Which statement BEST describes the distinction between a hydration and a dehydration reaction? a) Hydration requires a carbonyl group, and dehydration does not. b) Hydration is the addition of water, and dehydration is the loss of water. c) Hydration results in breaking bonds, and dehydration creates bonds. d) Hydration is an oxidation, and dehydration is a reduction. e) Hydration and dehydration actually describe the same process.

D The following compound would be classified as a (blank]. CH3-CH-CH₂-CH₂-CH3 1 OH O primary alcohol O secondary alcohol O tertiary alcohol O primary aldehyde Question 25 Which of the following compounds would have the highest boiling point? O CH3-CH₂-O-CH3 O CH3-CH2-CH2-CH3 O CH3-CH₂-CH2-OH O CH3-CH3

1. identify the non-covalent structural effects of organic compounds.