

Give the correct names for the structures drawn (i.e. A-D) or draw the structure for each of the names given (i.e.. E-F) for the compounds below. Draw the Lewis structure for each of the following compounds. [CHCCHCHCH(NH_3)CH_2CO_2]^pm (CH_3)_3CCH_2COCH(CH_3)CH[N(CH_3)_2]_2
6. From the names alone, draw the structure arrangement for the following organics a) Methane b) dichloromethane c) Ethylene (C2H4)
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]
draw the structure and the IUPAC names of the alkene products that would form in the acid catalyzed dehydration of 2,3-dimethyl-3-pentanol give them step mechanism for the formation of each product?,
2) Draw the molecular structure for the following IUPAC names? 2 Pts A) 2-Methylhexanoyl Chloride B) Ethyl butanoate 3) Rank the following radicals in order of decreasing stability (most stable to least stable). 2 Pts ton 11 IV Most Stable: : Least Stable 4) Fill in the blanks for the following reactions? 4 Pts ΕΙΟ, A) HEAT EU-I B) HEAT OH OH Diene Dienophile Ed
Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e., F-G) for the compounds below, and use the cis/trans, R/S labeling when appropriate.1a-Chloro-6-(trans) cyclobuty1 - 3- (cis) cyclohexyl-2-(cis) hydroxy-5-(rans) flouro-4-(cis) - (3 - Hydroxypropyl) cyclohexane
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)...
write the structure of the following compounda from their
IUPAC names
3. Write the structure of the following compounds from their IUPAC names: (a) ethanamide (b) methylethanoate (d) 2-butanone (c)propanoic acid (f) trimethylamine (e) methyl propyl ether
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., F) for the compounds below, and use the E/Z, cis/trans, equatorial/axial, R/S labeling when appropriate (Choose 4 overall which include A and E) он O2N NO2 CN NO2 Br Common Name (CH,)-СОНСОН(CH3)2 Common Name 4-Carbomethoxy-5-formyl-2-hydroxybenzenesulfonic acicd
5. Draw structure for the names and write the IUPAC name for the structures to points) Tho priority of functional groups for naming is: alkane < alkyl halide <ether <alkene alkyne < amine < alcohol ketone <aldehyde <carboxylic acid NH2 a. 3-chloro-4,4-dimethyl-1-nonen-6-yne d. (3E, 5Z)-2,6-Dimethyl-1,3,5,7-octatetraene