Page 6 of 21 vide the IUPAC name for each of the following compounds. OH -NO2...
Draw the condensed structural formula far each of the following compounds. a. 2-nonene b. 2, 3, 4-trimethylpentane c. trans-1-choro-3-ethylcycloheptane d. 4-isopropyloctane e. 1-bromo-2, 2-dimethylbutane f. cis-1-bromo-3-chlorocyclohexane g. g. A compound is incorrectly named 2-ethyl-2, 4-dimethylhexane. Draw the molecule and label with the correct IUPAC name.
1. Name the following compounds using IUPAC or accepted common name: 2. Draw a proper condensed, expanded or line-angle structures for the following compounds: /8 a. hepta-1,4-diyne b. cis-non-2-en-5-yne c. trans-6-chlorohept-2-en-4-yne
Please describe the iupac rules that lead to this name What is the IUPAC name for the following molecule? NO2 Selected Answer: Answers: d. 5-ethyl-2-nitrohept-4-ene a. 3-ethyl-6-nitrohept-3-ene b. 6-nitro-3-ethylhept-3-ene 2-nitro-5-ethylhept-4-ene d. 5-ethyl-2-nitrohept-4-ene 5-ethyl-2-nitrooct-4-ene e.
Question 6 (4 points) What is the IUPAC name of the given molecule? Br OH 4-ethyl-5-ol-hexanoyl bromide 1-bromo-4-ethyl-5-hydroxyhexanoic acid 4-ethyl-5-hydroxyhexanoyl bromide 4-ethylhexan-5-ol-1-carboxyl bromide Question 7 (4 points) Predict the product for the following reaction: (CH3),Culi HO et
Identify a systematic (IUPAC) name for each of thr following compounds 1. Identify a systematic (IUPAC) name for each of the following Compounds A NO2
- 6! Name the following compounds based on their structures (circle your answer) (6 pts tot сн. CH,CH.CH) a) eis-5-methylhex-2-ene b) trans-5-methylhex-2-ene eis-2-methylhex-3-ene d) trans-2-methylhex-3-ene 2) A - H _ CH CHCH a) 3-methylbut-3-ene 62-ethylprop-1-ene c)2-methylbut-1-ene d) 2-ethylprop-2-ene hepta-2,6-diene b) hept-2,6-diene c) hepta-1,5-diene d) hept-1,5-diene сн. (H,сне H a) (E)-3-methylhex-3-ene b) (Z)-3-methylhex-3-ene (E)-4-methylhex-3-ene a) (2)-4-methylhex-3-ene CHÚCH). a 3-methylcyclopentene $) methylcyclopentene c) 5-methylcyclopentene CH3 a) 2,5-dimethylcyclohexa-1,5-diene 1,4-dimethylcyclohexa-1,3-diene c) 1,4-dimethylcyclohexa-4,6-diene Hoa
Select the correct IUPAC name for the following branched chain alkane. CНз CH CH2CH2CH3 CH3CH CH2CH CH CH3 4-chloro-2-iodo-5,6-dimethylnonane 6-chloro-8-iodo-4,5-dimethylnonane 4-chloro-1-iodo-2,6,7-trimethyI nonane O 4-chloro-6-iodo-3-methyl-2-propylheptane Select the correct IUPAC name for the following branched chain alkane. CI СНCH-CH3 CHз CH3CH2—С— CH-CH2CHCHЗ CH2CH2CH3 4-(1-chloropropyl)-4-ethyl-7-methyloctane 3-chloro-4-ethyl-7-methyl-4-propyloctane 5-(1-chloropropyl)-2-methyl-5-ethyloctane O 6-chloro-5-ethyl-2-methyl-5-propyloctane Select the correct IUPAC name for the following cycloalkane: 1,3-diethyl-2-iodocyclohexane 2-iodo-1,3-dipropylcyclohexane 1-iodo-2,6-dipropylcyclohexane 2,6-diethy-1-iodocyclohexane Hint Select the correct IUPAC name for the following branched alcohol. OH CH3CHCH2CH2CНCH2CHCH3 CH2CH2CH3 CHз 2,7-dimethyl-4-decanol 2-methyl-7-propyl-5-octanol 4,9-dimethyl-7-decanol 7-methyl-2-propyl-5-octanol Select the...
CHM 211 STEREOCHEMISTRY Chapter 5 Write the IUPAC name for the following compounds and including the Rors configuration when appropriate? (1 pr. each) он CH.CH (a) HOCHB (d) H OH OH 10. Draw a dash-wedge structure for the following? (1 pt cach) (a) (1R)-1-bromo-1,3,3 trimethylcyclohexane (b) (2S,4S)-2-bromo-4-methylhexane 11. Draw fisher projection formula of (2S, 3R 45)-2,4-dichloro-3-methylhexane? (1)
4.23 4.25 156 CHAPTER 4 Woction to Organic Compounds 4.27 Give the correct IUPAC name for each following compounds: b. Br Practice Problems 4.23 Draw the condensed structural formula for each of the following groups: a propyl bmethyl 4.24 Give the correct name for each of the following substituents: 2. CH.CH b. CH3CH-CH-CH- c.- 4.25 Draw the skeletal structure for each of the following compounds: a. 2,3-dimethylpentane b. 2-ethyl-1,4-dimethylcyclohexane c. 1,2-dichlorohexane 4.26 Draw the skeletal structure for each of the...
Canvas 5 p Question 1 Provide an appropriate IUPAC name for the following compounds. OH (E) 4-hydroxy-2-octenone (Z) 4-hydroxy-2-octenone (Z) 5-hydroxy-6-octen-3-one (E) 5-hydroxy-6-octen-3-one