5. difference in pKa suggests that the reaction is more towards the reactant as the conjugate base is stable.
6.
these two alcohols are enantiomers formed in equal amounts.
4. option C is correct
A) 1-chronyhorthane B) 3-ethylphenol C) -ethyl-3-cyclohexaltiene-l-ol D) 1-hydroxyethylbenzene 4. The correct ranking for the following compounds...
d. AG-AH-AS/T 42. How many stereoisomers of 4-chloro-2-methylpentane (CHs):CHCH:CHCICHs, exist? a. I b. 2 c. 3 d. 4 43. What is the major organic product obtained from the reaction of 1-butanol with aqueous HBr at reflux? a. 1-bromobutane b. 2-bromobutane c. 2-bromo-1-butanol d. 1-butene 44. Which of the following alcohols reacts fastest with HBr to give the corresponding alkyl bromide? a. methanol b. ethanol 2-propanol d. 2-methyl-2-propanol C. 45.Which of the following alcohols undergoes the most H2SO4 to give rapid...
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
12) What is the product of the following reaction sequence? 0 1 SOC12 ) CH2CH2CH MgBr 2) H30* H A) 4-chloroheptane C) 3-chloro-4-heptanol B) 3-heptene D) 3-chloroheptane 13) _ 13) Which of the following cannot be made by the reduction of a ketone or aldehyde with NaBH4 in methanol? A) 2-methyl-2-propanol B) 1-butanol C) 2-methyl-1-propanol D) 2-butanol
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 please show the mechanism. I dont know how the hydrogens are moving in these reactions...
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...
amic dust obtained from the following race What is the major OH O TY A) 4 B)2 03 D)1 19. Provide an acceptable name for the compound below CHI CHA CHẠC,SH Bemethylho. 01 A) (2)-4-methylhex-3-ene-1-thiol B) (E)-4-methylhex-3-ene-1-thiol C) (2)-3-methylhex-3-ene-6-thiol D) (E)-3-methylhex-3-ene-6-thiol 20. What compound is formed when 2,2-dimethyloxirane is treated with ethanol containing a trace of HCI? A) 2-cthoxy-2-methyl-1-propanol B) 1-ethoxy-2-methyl-2-propanol C) 2-cthoxy-2-methyl-2-propanol D) 2-ethoxy-1-butanol E) 1-cthoxy-2-butanol 21. What is the major organic product obtained from the following reaction? A)...
1.) Which of the following compounds is chiral? A. 1-chloropentane B. 1,1-dichloropentane C. 2-chloropentane D. 2,2-dichloropentane E. none of these 2.) Compounds I and III are: A. enantiomers B. diastereomers C. structural isomers D. geometric isomers 3.) The molecules shown are: A. constitutional isomers B. enantiomers C. diastereomers D. identical E. none of these We were unable to transcribe this imageH3C
1. Which is the formula for an alkyne? a. CH3CH2CCH2 b. CH3CH2CH2CH3 C. CH3CH2CCH d. CH3CH2CCH2 2. Which of the following compounds is not possible? a. Brb. Bi C. Brd . BI, Br 3. What is the correct classification for the alcohol shown? CH3-CH=CH-CH-CH2 Сн,ОН a. Primary b. Secondary c. Tertiary d. Quaternary 4. Which of the following compounds is correctly classified as a tertiary alcohol? a. 3-methyl-1-butanol b. 2-methyl-1-butanol c. 3-methyl-2-butanol d. 2-methyl-2-butanol 5. Which of the following compounds...
QUESTION 18 Predict the product for the following reaction. OH 1. LiAIH4 2. H20 A. 3-methyl-2-pentanone B. 3-methyl - 1-propanol C. 2-methyl-1-butanol D.3-methyl-2-pentanol E none of these
1. Use a molecular drawing program to construct a balanced equation for the specific reaction of 2-propanol with the Lucas reagent including structural/skeletal formulas. Do not just copy the general reaction (no R's in your answer). 2. Use a molecular drawing program to construct an equation for the reaction of each of the specific alcohols in Part A (listed in Table 1) with chromic acid including structural/skeletal formulas. Write "No Reaction" for the products if no reaction occurs. Assume the...