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 structures for compounds named below. A) (Z)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne
1) Draw structures for compounds named below. A) (2)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne 2) Give IUPAC name for the following structure. 3) For each reaction below, indicate which starting material is the Nucleophile and which is the Electrophile. Show arrows to demonstrate how the transformation occurs. →^_^tts a Porto ~ onde gi 4) Draw a mechanism for the conversion of the shown starting material to the corresponding product. 5) In the transformation below, a starting material is treated with HCl to form...
draw the following compounds. A) (R)-4-methylpentane-1,2-diol B) cis-1-bromo-2-chlorocyclobutane c) (E)-1-fluoro-1,3-butadiene
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
lculate the degrees of unsaturation in the following compounds. a. C12H16N302Br b. C8H10C14 c. C9H20N4 d. C15H18 4. Draw structures for the following hydrocarbons. a. 3,5-diethyl-4-isopropyl-2,6-octadiene b. 4,5-dimethyl-1,4,7-decatriene c. 1-chloro-3-bromo-3-heptene d. 2-methyl-1,3-cyclopentadiene e. 4-isopropylcyclohexene
4. Draw the following cycloalkanes as two-dimensional structures, using wedges and dashes: trans-1-bromo-2-methylcyclopentane cis--chloro-3 ethylcyclohexane trans-1,3-dimethylcyclohexane trans-1-bromo-3 ethylcyclobutane cis-1-ethyl-4-methylcycloheptane cis-1-isopropyl-3- methylcyclopentane
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
4. Draw the line-angle structure for each of the following a) (2E,4Z)-4-ethyl-5-isopropyl-3,6-dimethylocta-2,4-diene b) (2Z,4Z,6E)-3-bromo-5-chloro-4-ethyl-7-fluoro-9-methyldeca-2,4,6-triene c) (5S,8S)-3-sec-butyl-5-ethyl-1,8-dimethylcycloocta-1,3,6-triene d) 2-ethyl-3,5,5-trimethylcyclopenta-1,3-diene
Draw all possible stereoisomers for each of the following.(a). 2- chloro-3-hexanol. (b). 2-bromo-4- chlorohexane . (c) 2,3,-diachloro pentane. (d). 1,3-diabromopentane.(2) .Draw the stereoisomers of 2-methylcyclohexane.
4. Provide resonance structure(s) for the following 5. Draw structure for: a) (2,3E)-3,4-dibromo-1-chloro-1,3-pentadiene b) E-3-bromo-2-hexene 27 Dashboard Calendar To Do Notifications Inbox