While drawing structures, first draw the carbon steel then place groups and functional groups at their respected positions.
Draw the following structures: 1. N-methyl-1-propanamine 2. N,N-dimethylmethanamine 3. 4,4-dibromohexano ic acid 4. 2-methylpentanoic acid 5....
only the circled ones please! 3 Write structural formulas for the following compounds 2,2-dimethylpropanoic acid 4-chloro-2-methylpentanoic acid (c) oxalic acid (d) ethyl acetate (e) acetic anhydride (f) x-iodobutyric acid (g) calcium acetate (h) m-bromobenzoic acid (i) isopropyl benzoate phenyl 5-methylhexanoate potassium propanoate 1 methyl 3,3-dimethylbutanoate (m) ethyl phosphate (n) isopropyl butanoate (o) 4-bromo-3-pentenoic acid
Draw structures corresponding to the following names: 9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne 9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
Questions 1. Draw the structure of methyl salicylate, and say what evidence indicates that methyl salicylate was formed. 2. Draw and compare the structures of acetylsalicylic acid and methyl salicylate. Circle and name the functional groups in both compounds. 3. The fragrance of apricots is due to the ester pentyl butanoate. Write the equation for the synthesis of this ester from the acid and the alcohol. 4. Give examples and names of any other compounds that contain the functional groups...
Provide structures for the following: 4,4-dimethyl-2-pentyne 5,5-dimethylnon-3-yne 4,5,5-trimethyl-2-hexyne 1-penten-4-yne 1-cyclohexylethyne propyne 4-isopropyl-2-methyl-1-nonene 6-ethyl-3-nonyne
1) Draw the structure for each named compound: a) (Z)-N-ethyl-3-bromo-2-isopropyl-5- b) propanoyl chloride methyl-2-hexenamide c) benzoic anhydride d) (R)-3-chloro-4-ethylhexanoic acid e) ethyl 4-methylpentanoate f) pentanenitrile g) cyclohexanecarboxamide h) octyl butanoate 2) Provide an IUPAC name for each structure: b) 9 CH d) CH.CH нс снсон TH Page
Draw the structures of the following carbonyl compounds: 4-hydroxypentanoic acid ethyl ethanoate methyl 2-aminobenzoate 4-bromocyclohexanone 1-bromo-2-chloro-cyclopentane carboxylic acid
2. Draw structures of the compound based on the given IUPAC name 1) (2E,5E-N-ethyl-N-methylhepta-2,5-dienamide 2) (1R,2R,3R,5R)-1-ethyl-5-isopropyl-3-methyl-2-(3-methylpentyl)cyclohexane Identify aromatic ring system 3. 2. Draw structures of the compound based on the given IUPAC name 1) (2E,5E-N-ethyl-N-methylhepta-2,5-dienamide 2) (1R,2R,3R,5R)-1-ethyl-5-isopropyl-3-methyl-2-(3-methylpentyl)cyclohexane Identify aromatic ring system 3.
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
Page of 11 1. Draw structures for the following molecules: ZOOM 5, 5-dimethyl-3-hepten-1-al 2-amino-3-isopropyl-1-butanoic acid 2, 4, 6-tribromo-1, 3, 5-trinitro cyclohexane 3-methoxy-2, 5-hexanedione N-ethyl-N, N-dimethyl amine 3, 4-dihydroxy-1, 6-hexanedioic acid 1-cyano-6-nitro-3-phenyl-4, 7-nonadien-2-one (2R)-2-amino-2-mercapto-4-pentene MacBook Air F 44 F2 FS * & % $ 7 6 5 4 3 2 P Y T R E W Q O
9.4 Draw a structural formula for each of the following esters: a. cyclohexyl propanoate b. methyl formate e, ethyl benzoate d. isopropyl acetate e. butyl butanoate f. propyl pentanoate 9.5 Assign names to each of the following amines: NH b. CH, -NH-CH2-CH c. (CH-CH2),N 4. NH - CHE 6, CHỊCH,CH, NH, 9.6 Complete the following equations: a. CH CH NH2 + HCI NH b. + HCI C. CHỊCHÚNH - CHI + HBr + d. N(CH)2 + HBr - 9.7 Draw...