1) Amino group is Primary because the nitrogen is attached to only one carbon atom .(Primary amines have only one carbon bonded to nitrogen.)
2) Alkylbromide group is Tertiary because carbon attached to bromine is further attached to three carbon atoms so the alkyl Bromide group is tertiary .
3)Methyl group is Secondary because carbon attached to methyl group is further attached to two carbon atoms so the methyl group is secondary .
4) Alcohol group is Secondary because carbon attached to alcohol group is further attached to two carbon atoms so the alcohol group is secondary .
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Explaination
First right 7 carbons side-by-side because in the given name the parent chain contain 7 carbon due to the presence of hept in the name.
Number these carbons from left to right as 1 2 3 4 5 6 7
The Amino substituent is at 5th carbon of this carbon chain
The bromo substituent is present on the the 3rd carbon of this carbon chain
The methyl substituent is present at the 3rd carbon of this carbon Chain and
alcohol group is present at 2nd position and it is the functional group therefore written at the end of the name as 2-heptanol . (-ol is written to denote alcohol or hydroxyl group /OH-)
After writing all the substituents and functional group Now add hydrogens to complete the valency of 4 of all the carbons .
8. Draw the structure of 5-amino-3-bromo-3-methyl-2-heptanol. Classify the alcohol, amine and alkyl halide present in this...
3. Draw and classify the following alkyl halides as methyl-, primary (1°), secondary (11°), or tertiary (111°) halide: 10pts -2-chloro-3,3-dimethylhexane; -4-sec-butyl-2-chlorononane; -1-bromo-4-isopropylcyclohexane; -2-chloro-3,3-dimethylhexane; -4-sec-butyl-2-chlorononane; -1-bromo-4-isopropylcyclohexane;
Please answer in detail 1. Classify the following cation, alkyl halide, and alcohol as either primary (1°), secondary (2º), tertiary (39) or но"
Draw the structural formula for a compound that contains a tertiary alcohol, a secondary alkyl halide, and primary, secondary and tertiary hydrogens. a. Indicate the number of beta-hydrogens relative the alkyl halide. b. Name the compound you just drew.
2 Rob page 6 Part B: 3 1. Classify the following cation, alkyl halide, and alcohol as either primary (1"), secondary (2) or tertiary (3) HO 2. Write the major product(s) A, B and C for the following transformations: RUBH NaOH, HO2 С Br2 NaOH ( excess) B А
1. Draw the structure of any secondary alkyl halide containing at least six carbons. 2. Name it. 3. Circle the alpha carbon. 4. Draw box around all the beta carbons. 5. Draw the product(s) for the elimination reaction product for your choosen alkyl halide.
1. Draw the structures of the following alcohols: ethanol 2-propanol cyclohexanol 2-methyl-2-propanol Classify each of the alcohols in question 1 as primary, secondary, or tertiary. ethanol 2-methyl-2-propanol 2. 2-propanol cyclohexanol 3. Which alcohol would you expect to be more soluble in water, 1-butanol or 2-methyl-2- propanol? Why? (Hint: draw both alcohols examine their structures).
Be sure to answer all parts. Draw the structure of 4-methyl-2-heptanol. Then draw and name the product that you would expect to produce by its oxidation. Part 1: Structure of 4-methyl-2-heptanol: view structure Part 2: Structure of oxidation product: no structure shown Part 3: Name of product: 4-Methy-3-heptanal 4-Methylheptanone 4-Methyl-3-heptanone 4-Methyl-2-heptanone
HO Regarding the following reaction: 1) a. Classify the alkyl halide as tertiary, secondary, or primary. b. Based on your answers to la, deduce whether the alkyl halide would be suitable for (i) only S2 reactions, (ii) only Ss 1 reactions, or (1) both/either S2 or S1 reactions. 2) a. Classify the nucleophile (the electron-sharer) as either strong or weak b. Based on your answer to 2a, deduce whether the nucleophile would be suitable for (i) only Sw2 reactions, (1)...
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
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