catalyst The steric strain in the trisubstituted alkene makes the reaction exergonic. O The reaction is exergonic due to the reduction in angle strain in the product. O The alkene in the product has more stable bonding thane alkene in the starting material. O The use of the catalyst makes the reaction exergonic. O The product is more stable than the starting material making the reaction endergonic.

catalyst The steric strain in the trisubstituted alkene makes the reaction exergonic. O The reaction is exergonic due to the reduction in angle strain in the product. O The alkene in the product has more stable bonding thane alkene in the starting material. O The use of the catalyst makes the reaction exergonic. O The product is more stable than the starting material making the reaction endergonic.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterNW2: Nomenclature Worksheet 2: Intro To Naming Functional Groups

Section: Chapter Questions

Problem 4CTQ: Draw the following alkenes: a. 2,3-dimethylbut-2-ene b. cyclopenta-1,3-diene c. penta-2,3-diene

See similar textbooks

Similar questions

Which statement is true about the isomerization reaction below? catalyst O The use of the catalyst makes the reaction exergonic. O The alkene in the product has more stable bonding than the alkene in the starting material. O The product is more stable than the starting material making the reaction endergonic. O The steric strain in the trisubstituted alkene makes the reaction exergonic. O The reaction is exergonic due to the reduction in angle strain in the product.
the bonds in the alkene compounds are sigma and bi bonds true or flase
Draw the following alkenes: a. 2,3-dimethylbut-2-ene b. cyclopenta-1,3-diene c. penta-2,3-diene
The following alkene is: O primary O monosubstituted O disubstituted secondary
Identify the major product of this reaction of an alkene. | ||| OH OH 1. Hg(OAc)2, H2O 2. NaBH4, NaOH || IV ㅊ OH OH
Name each alkene. a. CH;=CH-CH;-CH3 CH, CH3 b. CH3-CH-c=CH-CH3 c. CH,=HC-CH–CH,-CH,-CH, CH3-CH ČH3 CH3 d. CH3-CH-CH=C-CH3 CH,-CH3
Name each alkene. a. CH;-CH,-CH=CH-CH,-CH; b. CH,-CH-CH=CH-CH, CH3 CH; CH, c. CH,-CH-CH=C-CH-CH, CH3 CH; CH, d. CH;-C-CH=C-CH2-CH, CH3
Zaitsev's rule: states " The alkene formed in greatest amount is the one that corresponds to O A. removal of the hydrogen from the alpha-carbon having the fewest hydrogen substituents O B. removal of the hydrogen from the any-carbon having the fewest hydrogen substituents OC. removal of the water molecule from the alpha-carbon having the fewest hydrogen substituents D. removal of the hydroxyl (OH) from the any carbon having the fewest hydrogen substituents O E. addition of hydrogen to more substituted carbon atom Reset Selection Previous Next Save 26°C Sunny DELL 立

Vhich of the following statements is incorrect? * 3 p Hammond-Leffler Postulate states that there is a strong resemblance between the transition state and the product in an endothermic reaction. Hammond-Leffler Postulate states that there is a strong resemblance between the transition state and the reactants in an exothermic reaction. The presence of more electron-donating alkyl groups ineffectively delocalize the positive charge in an organic molecule, making it less stable. The dehydration of primary alcohol proceeds via E2 mechanism. All of the abovę
7. List the products of each alkene addition reaction. a. CH;-CH=CH-CH, + Cl b. CH;-CH-CH=CH-CH, + HBr CH, c. CH;-CH2-CH=CH-CH, + Brz CH3 d. CH;-CH-CH=C-CH3+ HCl
Rank the alkenes from most stable to least stable.
In free-radical substitution reaction of alkanes with halogens under uv light, the photolytic breaking of the halogen is the rate determining step. the formation of alkylradical is the rate determining step. the formation of halogen radical is the rate determining step. the abstraction of hydrogen from alkane by the halogen radical is the rate determining step