3. Explain why the following name is unsatisfactory, and give a correct name (8 pts). (a)...
14) What is the name of the major product of the following reaction? н", Н,0 CH2=CHC(CH)3 A) 2,3-dimethyl-1-butanol B) 2,3-dimethyl-2-butanol C) 3,3-dimethyl-1-butanol D) 3,3-dimethyl-2-butanol E) 4-methyl-2-pentanol
Give the IUPAC name for the following compounds. 3, 3 diethyl dimethyl ethyl methyl butanol pentanol hexanol
What is the IUPAC name of the following compound? OH (R)-2.2-dimethyl-3-pentanol (5)-2.2-dimethyl-3-pentanol 1-tert-butyl-1-propanol (S)-4,4-dimethyl-3-pentanol Question 25 What is the IUPAC name of the following compound? OH t (E)-5-methyl-2-hexen-5-ol (Z)-5-methyl-4-hexen-5-ol (E)-2-methyl-4-hexen-2-ol (Z)-2-methyl-4-hexen-2-ol
Select the correct IUPAC name for the following branched alcohol. Select the correct IUPAC name for the following branched alcohol. CH3CHCH2CHCH2CH2CH2CH3 CH2CHCH2CHCH2CH3 CH3 CH2CH3 O 3-butyl-7-ethyl-1,5-dimethyl-2-nonanol 7-methyl-9-ethyl-5-(2-hydroxypropyl)undecane 4-butyl-8-ethyl-6-methyl-2-decanol 7-butyl-3-ethyl-5-methyl-9-decanol O
8. Circle the answer. Which is the correct IUPAC name for the following compound? OH A. 4-Isopropyl-1,1-dimethyl-1-pentanol B. 5-Isopropyl-1,1-dimethyl-2-hexanol C. 1,1,4,5-Tetramethyl-1-hexanol D. 3,5,6-Trimethyl-2-heptanol E 2,5,6-Trimethyl-2-heptanol 9. A chemist attempted unsuccessfully to form iodoethane from ethanol using Nal. Why did the reaction fail? A. I was not a good enough nucleophile. B. A secondary or tertiary alcohol was needed. c. OH is a poor leaving group. D. Na was a poor counterion.
Which is the correct name for the molecule depicted below? CH2-CH3 CH-CH-CH2-OH CH, CH, Multiple Choice O 3-ethyl-2,3-dimethyl-1-propanol O 2,3,4-trimethyl-1-butanol O 2,3-dimethyl-1-pentanol O 3,4-dimethyl-5-pentanol
I only need help with question #2 but insight into the rest of them would be very helpful. Draw the structure of the aldehyde or ketone you could reduce to give the following a. benzyl alcohol b. 3,3-dimethyl-2-butanol c. 3-methyl-1-butanol d. cyclohexanol. 2. Draw the most stable conformation of the following molecule i.e draw the most stable chair. Use the convention for sugars. Why is it the most stable? 3. Are the cis and trans isomers of 4-tert-butyl cyclohexanol chiral?...
please explain fully. also I am confused why there are numbers in with E and Z (2.) Draw structures corresponding to the following names: a) (4E)-2,4-dimehyl-1,4-hexadiene b) Cis-3,3-dimethyl-4-propyl-1,5-octadiene c) 4-methyl-1,2-pentadiene d) (3E,5Z)-2,6-dimethyl-1,3,5,7-octatetraene e) 3-butyl-2-heptene f) Trans-2,2,5,5-tetramethyl-3-hexene
8. (8 pts) Give the correct IUPAC name for the following compounds a) Br b) 9. a) (5 pts) What is the major product of the following reactions sequences?
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: CHCH2 a CHCH2 II III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1,5-octadiene (3Z,SE) -26-dimethyl-1,3,5,7-octatetraene 4-methyl-1,2-hexadiene