Explain why an amide ion cannot be used to form a carbanion from an alkane in a reaction that favors products.

Draw the structure for this organic compound

Draw the structure for 2,2-dimethyl-4-propyloctane.

Which functional category CANNOT be an ester's isostere? carbamate. amide urethane.   pyrrole.

Which of these does not occur in a substitution reaction? Carbon atoms are bonded to a different number of atoms in the product than in the reactant Aromatic hydrocarbons will undergo substitution reactions with chlorine and bromine in the presence of a catalyst A hydrogen atom or functional group is replaced by a different atom or functional group Two compounds react to form two different compounds A alkyl halide can undergo a substitution reaction with a hydroxide ion to produce an alcohol

Which of the statements are true? 1. Aldehydes readily undergo oxidation to carboxylic acids 2. Propanone and acetone are two names for the same compound 3. The benedicts test distinguishes between aldehydes and ketones

What is the difference between the C=O bond in aldehydes and ketones?

Hydrolysis of an ester (in presence of acid catalyst) forms --- and ---.   Question 16 options:   a carboxylic acid, an alcohol   an alkene, an alkane   a carboxylic acid, an alkene   an aldehyde, a ketone

Write the structural formula for the product(s) of the following reactions.    N-ethyl propanamide + KOH ⟶

Ketones, aldehydes, carboxylic acids, esters, and amides all have a carbon-oxygen double bond (often called a carbonyl group). Explain how these classifications of organic compounds are different from each other.