

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 the structures to the corresponding to the names? Benzyl benzonate, N-methyl-N propyl-2-butanamine, Methylcyclobutanecarbon nitrate, 24-Pentanedione, Bromo 2-chloro 1-butanol, Ethyl 1-ethylpropyl ether, Cyanoacetic acid, 3-Phenzyl2- hexenal , -4- Methyl-3-hexen-2-one Rank the following groups of compounds from most acidic to least acidic. Place the number corresponding to the compound's relative rank in the blank below the stucture. (CF3)2CHOH (CH3)3COH CH3CH2OH
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]