2) Use compound C (shown below) to answer the following questions. H2N CH, H compound C H3C Br a) Classify compound C as a primary, secondary or tertiary amine. b) Give the IUPAC name for compound C, omitting absolute configuration (R or S) designations. c) In the indicated spaces below, draw the enantiomer, a diastereomer and a Fischer projection of compound C. enantiomer of compound C diastereomer of compound C Fischer projection of compound C

1).  For each o the following, draw one structural formula that meets all stated requirements,then name each structure you drew according to either IUPAC or common nomenclature.

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In an attempt to synthesize compound C through a two-step process, a chemist discovered after completing the first step that they had inadvertently produced two distinct compounds, A and B. Upon examining the infrared spectroscopy (IR) results, it was observed that both A and B exhibited peaks indicative of a ketone and an ester group. Please provide the molecular structures of A and B. OEt NaOEt ΕΙΟ A B In a chemical experiment, they noticed that both components, A and B, from a combined sample turned into a new compound, C, during the following stage. The task is to determine what compound C looks like and explain how compound A or B changes into compound C through a reaction. Compound C should be the primary molecule containing carbon created in this process, not just a by-product. A B H3O+, H₂O, A Mechanism = с

Both the melting point and boiling point of acetamide are higher than those of its N,N- dimethyl derivative. How do you account for these differences? CH,CNH, CH,CN(CH3), N,N-Dimethylacetamide mp -20°C, bp 165°C Acetamide mp 82.3°C, bp 221.2°C

Identify the IUPAC name of the given compound.   a)  2-methyl-3-amino-1-cyclopentanone   b)  1-amino-2-methyl-3-cyclopentanone   c)  3-amino-2-methyl-1-cyclopentanone   d)  2-amino-1-methyl-2-cyclopentanone

19.62 Naltrexone is used to help recovering narcotic addicts stay drug free. HO O OH naltrexone LO1,6,7 (a) Label and name all the functional groups. Where relevant, indicate whether the group is primary, secondary or tertiary. (b) Upon addition of dilute hydrochloric acid solution, naltrexone forms a water-soluble salt. Draw the structure of this salt.

This question has multiple parts. Work all the parts to get the most points. Answer true or false. a In the IUPAC system, primary aliphatic amines are named as alkylamines. true false b The IUPAC name of CH3 CH₂ CH₂ CH₂ CH₂NH2 is 1-pentanamine. true false C 3-Pentanamine is chiral and shows enantiomerism. true false dN-Ethylpropylamine is a 2º aromatic amine. true false Submit Answer Try Another Version 3 item attempts remaining

3. Which of the following is a hemiacetal? A) CH³. CH CH CH³ B) OCH,CH3 CH3-C-H OH OCH, C) HOCH,CHCH,CH3 D) ove Lasr checked Cop