1) Draw structures for compounds named below. A) (2)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne 2) Gi...
1) Draw structures for compounds named below. A) (Z)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne
Draw structures for the following compounds. a. 2-chloro-1,3-cyclopentadiene b. 2-bromo-5-nitroaniline c. 2-chloro-5-fluoro-3-octyne
1. Draw the compounds named below. (3R)-3-chloro-2-methylpentane (1R, 3S)-1-bromo-3-ethylcyclohexane 2. Draw the mechanisms for the reactions shown. Br XX- Br ~ SH - SH 1
The correct IUPAC name for the compound shown below is: CH3 O2-bromo-6-methyl-3-heptyne O2-bromo-6-methyl-3-heptane O 6-methyl-2-bromo-3-heptyne O2-bromo-6-methyl-3-heptene O 6-bromo-2-methyl-4-heptyne
1. 3-methyl-1-butene on reaction with H-Cl forms two products, namely 2-chloro-3- methylbutane (minor) and 2-chloro-2-methylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 2. 3,3-dimethyl-1-butene on reaction with HBr forms two products, namely 3-bromo-2,2- dimethylbutane (minor) and 2-bromo-2,3-dimethylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 3. Calculate...
17) Provide the proper IUPAC name for the alkene shown below 3-boro, A mutin agionavane 18) Provide the proper IUPAC name for the alkene shown below CH" 19) Draw an acceptable structure for 4-phenylbut-1-ene. 20) Draw an acceptable structure for 1,2-dimethylcyclohexene. 21) Draw and name all alkenes which have the molecular formula C4Hs. 22) Name the alkene shown. Be sure to include the appropriate E or Z label necessary CH,CH 22) 23) 23) Provide a correct IUPAC name for the...
Draw the structures for the following compounds. a) (3Z,5S)-4-bromo-5-chloro-2-methylhexa-1,3-diene b) (5S,7S)-5-(bromomethyl)-7-chloro-oct-2-yne c) (1S,5S,6S)-6-bromo-5-[(1R)-1-chloroethyl]cyclohex-3-enol d) 2-bromo-4-[(1R)-1-hydroxyethyl]benzoic acid e) (3S,4S,5S)-5-amino-3-hydroxy-4-methylhexanal f) (Z,2R,4R)-6-bromo-4-chloro-N-ethyl-N-methylhept-5-en-2-amine g) [(1S)-1-chloroethyl] (Z,3R)-5-chloro-3-methoxyhex-4-enoate h) (Z,3R)-3-bromo-4-chloro-7-methyloct-4-enoic acid i) (3S)-6-bromo-N-ethyl-N,3-dimethylhex-4-ynamide j) (Z,3R,4S)-6-bromo-3-[(1S)-1-chloroethyl]-4-hydroxyhept-5-en-2-one
draw the following compounds. A) (R)-4-methylpentane-1,2-diol B) cis-1-bromo-2-chlorocyclobutane c) (E)-1-fluoro-1,3-butadiene
4) Draw the following compounds a. (2S,5R)-5-chloro-2-ethylhexanoic acid b. (1R,2R,4R)-4-ethylcyclohexane-1,2-diol c. (2S,3R)-3-amino-2-phenylbutanal d. (1S,2S,3R)-2-fluoro-3-propylcyclobutanol e. (2E, 7Z)-5-bromo-2,7-nonadiene
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