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d. AG-AH-AS/T 42. How many stereoisomers of 4-chloro-2-methylpentane (CHs):CHCH:CHCICHs, exist? a. I b. 2 c. 3...
Give the Line Drawing for the followingg (g) 1-chloro-3-methylbutane (h) pentane (1) 2,3-dichloro-2-methylpentane ) 2-chloro-2,4,4-trimethylpentane(k) trichloromethane ()2-butanol (m) 3-methylpentane (n) 3-bromo-2-methylpentane (o) 3-ethylhexane (p) 5-isopropyl-3-methyloctane (q)3,3-dibromo-1,1,1-trichlorobutane (r) cis-1-bromo-2-pentene (s) 2,5-dimethyl-1-hexene (t) 2,5,5-trimethyl-3-heptyne (u) trans-1,2-dibromo-1-butene (v) 2-ethyl-1-butene (w) 5-bromohept-6-en-3-ol (x) 5-methyl-4-hexen-1-yne (v) 3,3-dimethyl-1-butanol (z) butane
A) 1-chloro-4-methylpentane B) 2-chloro-4-methylpentane C) 2-chloro-3-methylpentane D) 3-chloro-2-methylpentane E) 2-chloro-2-methylpentane Arrange the compounds above in order of greatest reactivity to least reactivity for an SN2 reaction [Select) [Select) [Select] [Select) [Select]
1- isopropanol (also known as 2-propanol) is formed primarily from the hydration reaction of an alkene. The alkene is [ ] 2- When the O in an alcohol is replaced with a sulfur atom, the resulting compound is called a(n) [ ] 3- The dehydration of two primary alcohols results in a(n) [ ] A alkene B aldehyde C carboxylic acid D ester E ether 4- Fill in the blank. CHCHCHC≡CCHCHCl is named _______. A 7-chloro-4-heptyne B 5-chloro-2-heptene C 1-acetylenenyl-3-chloropropane...
A) 1-chloro-4-methylpentane B) 2-chloro-2-methylpentane C) 3-chloropentane D) 2-chloro-3-methylpentane Arrange the compounds above in order of greatest reactivity to least reactivity for an SN1 reaction. Select Select) Select Select)
Question 10 10 pts A) 1-chloro-4-methylpentane B) 2-chloro-2-methylpentane C) 3-chloropentane D) 2-chloro-3-methylpentane Arrange the compounds above in order of greatest reactivity to least reactivity for an SN 1 reaction. Select 4 | Select) • , (Select Select)
- 1. How many stereoisomers exist for 2-chloro-3-methylpentane? 1.now 2. Which of the following substituents has the highest priority? A. -COOH B.-CHOC.-CH,OH D. -CH, 3. Which of the following have the S configuration? HO- E. only i and ii G. only ii and iii A. only i B. only ii c. only iii D. all _4. Enantiomers would have the same: A. melting point B. solubility in CCI C. rotation of plane polarized light D. all of the above E....
5. Explain how the following changes will influence the rate of the reaction of 2-bromo-2- methylbutane with methanol: a. The alkyl halide is changed to 2-chloro-2-methylbutane b. The alkyl halide is changed to 2-chloro-3-methylbutane 6. What product(s) do you predict for the following reactions? Be specific with regard to stereochemistry. Also, indicate which stereoisomer will be more predominant. a. R-2-bromopentane + CH30 b. R-3-bromo-3-metylheptane + CH3OH C. 1-bromo-2-butene + CH30 d. 1-bromo-2-butene + CH3OH e. E2 reaction of 2-bromobutane f....
Draw all possible stereoisomers for each of the following.(a). 2- chloro-3-hexanol. (b). 2-bromo-4- chlorohexane . (c) 2,3,-diachloro pentane. (d). 1,3-diabromopentane.(2) .Draw the stereoisomers of 2-methylcyclohexane.
Identify the alkene obtained on dehydration of each of the following alcohols: (a) 3-Ethyl-3-pentanol (b) 1-Propanol (c) 2-Propanol (d) 2,3,3-Trimethyl-2-butanol
Consider 2,4-dichloro-3-methylpentane: How many stereoisomers are possible for this compound? a)8 b)6 c)4 d)3 e)2