Last option (d) seems correct as this belongs to secondary amine. Secondary amine contains -NH- group.
Configuration Content%7C 135106721%21Coursel.C_1071570.1%21Coursemer 2. Select the secondary amine: O 1-propanamine O 2-propanaine O N,N-diethyl-2-butanamine O N.propyl-2-propanamine
2. Select the secondary amine: O 1-propanamine O 2-propanaine O N,N-diethyl-2-butanamine O N-propyl-2-propanamine MacBook
2. Select the secondary amine: 1-propanamine 2-propanaine N,N-diethyl-2-butanamine N-propyl-2-propanamine
Meme File Edit View History Bookmarks Window Help 3. Select the tertiary amine: 3.propanamine O 3-octananaine O N,N-diethyl-1.pentanamine O trimethylammonium chloride OOO
Give the common name for the amine N,N-diisopropyl-2-butanamine
1.What could be an alternate name for 2-aminobutane? Question 1 options: terbutyl amine isobutyl amine 2-butanamine 1-butanamine 2.Which pairing of general formula and compound class is incorrect? Question 2 options: R3CNH2; tertiary amine. RC=O NH2; amide. R2NH; secondary amine. RNH2; primary amine 3.Which of the following is not a primary amine? Question 3 options: 3-Hexylamine. Cyclohexylamine. Diethylamine. 1-Butylamine 4. When many copy molecules of the amine below are explored, which of the following amines do you expect NO to make...
O EtOCOET H N Eto EtOH Reactions of a primary or secondary amine with diethyl carbonate under controlled conditions gives a carbamic ester. Write a detailed mechanism for this reaction (shown above) which proceeds in 4 steps, including proton transfer steps. Then draw Intermediate 3 in the window provided. The mechanism is detailed as follows: Step 1: Nucleophilic attack to yield zwitterion intermediate 1. Step 2: Protonation/deprotonation (i.e. "proton transfer") of zwitterion 1 to yield intermediate 2. Step 3: Intramolecular...
Select the single best answer. Classify m-chloroaniline as a primary, secondary, or tertiary amine. O Secondary amine Tertiary amine Primary amine
Draw the structures of the following compounds. Classify each compound as a primary, secondary, or tertiary amine, or as a quaternary ammonium salt. 3-ethyl-N- 2-methyl-2-propanamine N-methyl-2-propanamine methylcyclohexanamine 1° amine 2º amine O 3ºamine 4º ammonium salt 1° amine O 2º amine 3º amine O 4º ammonium salt ОООО 1º amine 2º amine 3º amine 4º ammonium salt
Design a synthesis of 2-ethyl-N,N-dimethyl-5-hexen-1-amine from any cyclic secondary amine containing only C, H, and N. CH₃ any cyclic secondary amine containing only C, H, and N CH3 1 1 Part 1 out of 6 Choose the best option for the immediate precursor to the target molecule. CHE N CH3 A H C CH3 N CH3 CH3 C HCTCH, © Br. CH3
Draw the structures of the following compounds. Classify each compound as a primary, secondary, or tertiary amine, or as a quaternary ammonium salt. 2-methyl-2-propanamine 1 degree amine 2 degree amine 3 degree amine 4 degree ammonium salt N-methyl-2-propanamine 1 degree amine 2 degree amine 3 degree amine 4 degree ammonium salt N-methylpiperidine 1 degree amine 2 degree amine 3 degree amine 4 degree ammonium salt