Is cis-4-methyl-2-pentene makes stable carbocation reacting with HCl than trans-4-methy-2-pentene?
Is cis-4-methyl-2-pentene makes stable carbocation reacting with HCl than trans-4-methy-2-pentene?
#4. 2-pentene and 2-methyl-2-butene are not isomers stereoisomers constitutional isomers cis and trans isomers #6. Bromination of cyclohexene gives 1,2-dibromocyclohexane 1,1-dibromocyclohexane bromocyclohexane 1,2-dibromocyclohexene
Explain why 3-methylcyclohexene is more stable than methylcyclohexane. ОН HA -H20 2-Methylcyclohexanol cis, and trans) 3-Methyl- 1-Methyl Methylene- cyclohexene cyclohexene cyclohexane
Which of the following would be the products of an SN2 substitution of trans-1- chloro-4-methyl-cyclohexane reacting with hydroxide? trans-4-methyl-1-cyclohexanol cis-4-methyl-1-cyclohexanol A. trans-4-methyl-1-cyclohexanol D. 1-methyl-1-cyclohexanol B.cis-4-methyl-1-cyclohexanol C. a 50:50 mixture of the cis and trans products
2. Draw the structures of the cis-trans isomers for each compound. Label them cis and trans. If no cis-trans isomers exist, write none. a. 2,3-dimethyl-2-pentene b. 1,1-dimethyl-2-ethylcyclopropane c. 1,2-dimethylcyclohexane d. 5-methyl-2-hexene e. 1,2,3-trimethylcyclopropane
2.1. Name the following compound. Specify cis/trans geometry, if applicable. Q.2. Draw line structure for cis-4-methyl-2-hexene. 03. Draw a strucrure with molecular formula CH,20 which exhibits cis/trans isomerism, and also has a chiral center. How many stereoisomers are possible for this molecular formular? Q.4. What is the index of hydrogen deficiency of a compound with molecular formula C-H, BINO? Q.5. How many stereoisomers of 4-chloro-2-pentene exist? a 1 6 . 2 c. 3 d. 4.
What is made when 4-methyl-2-pentene reacts with HCl?
1 11-15. Determine the relationship between the following pairs of compounds. 11 trans-2-pentene and cis-2-pentene A) structural isomers 12. trans-2-pentene and cyclopentane B) Enantiomers C) not related 13. hexane and 2-methybutane D) same molecule 14. trans-2-heptene and trans-2-hexene E) geometrical (cis/trans) isomers 15 glycerol and 1,2-ethandiol (stereoisomers)
The reaction of 2-pentyne with Na/NH3 gives the following product: (1) cis-2-pentene (2) trans-2-pentene (3) 1-pentyne (4) pentane
Provide the following Draw cis 2-pentene Draw trans 2-pentene Draw a structural isomer 2-pentene Draw 2 alcohols that would produce 2-pentene with dehydration (you would get a mix of cis and trans) Draw a compound with 5 carbons that is not related to 2-pentene
i know that trans is more stable than cis but i really confusion between 2 and 4. please give me the answer with clear explanation and clear writing. i dont know anything about bulky group 5. Which of the following is the most stable conformation of trans-1-ethyl-3-methylcyclohexane? CH.CH CH2CH3 ÇH CH3 CH3 CH2CHE CH2CHE - C O (A) 1 (B)2 O(C) 3 O (D) 4