2. In the boxes below, draw structures corresponding to the following names. Please use proper line-angle...
[8 marks] 1. In the boxes below, draw the resonance structures of the organic radical intermediate of the given reaction, along with the two different products (constitutional isomers) that would be produced. No electron-flow arrows are required at any time. Stereochemistry is not required. Note: NBS N-bromosuccinimide Organic reaction intermediate NBS hv Product 2 Product 1 [6 marks 2. In the boxes below, draw structures corresponding to the following names. Please use proper line-angle
13. Draw line-angle structures corresponding to the following IUPAC names: (15, 2R)-1,2-dibromocyclopentane
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
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e.. T) for the compounds below, and use the cis/trans, R/S labeling when appropriate. E T D F 1a-Bromo-2-(trans) Chloro-4-(trans) Ethyl-3-(trans) Methyl-6-(Cis) 2-Hydroxypropyl-5-(trans)- (n-Propyl) Cyclohexane. Note, all of the groups orientations are in reference to la-Bromo Group all of the conformers specifications (e.g., axi the chair conformers of 1)- Give the correct names for the structures drawn (i.e. A-E)...
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
10.18 Draw structures corresponding to the following IU PAC names (a) 2,3-Dichloro-4-methylhexane (b) 4-Bromo-4-ethyl-2-methylhexane (c) 3-lodo-2,2,4,4-tetramethylpentane (d) cis-1-Bromo-2-ethylcyclopentane
2. Draw the structures corresponding to the following IUPAC names: a. 1,1-Dimethylcyclooctane b. 1,3-Dibromo-5-methylcyclohexane Stereochemistry of Cycloalkanes: Identify the following cyclodtkanes as Cis or Trans then name them according to IUPAC rules Br CI
help please! Draw the Fischer projection for (2S, 4R)-2-bromo-4-ethyl-4-methyloctane 13. (6) Draw the line-angle formula for: (4R, 5S), 2,4,5-trimethylheptane
Give the correct names few the structures drawn (i.e. A-C) or draw the structure for each of the names given (i.e., D) for the compounds below. 1-Bromo-2-chloro-3-methylcyclopropane Draw the Lewis structure for the compound given below. A) [H_3NCH_2CHC(CH_3)CCCHF_2]+ B) (H_3C)_2CHCH_2CH[C(CH_3)_3]CH_2CH(CH_3)_2 c) [CH_2CHOCCF_2CO_2CH_2CH_2OOCH_2CH_2CO_2]
Provide the structure for the following compounds given the IUPAC names. Use dashes and wedges to show R and S. (2S, 4S, 6S)-2-bromo-4, 6-diethyloctane (1R, 3R, 5S)-1-bromo-3-chloro-5-isobutylcycloheptane