0
The stereochemistry of the hydroboration mechanism is. a. anti-Markov b. Markovnikov addition c. syn addition d. anti addition?
Wiki User
∙ 14y ago
It's anti markownikoff addition
Wiki User
∙ 14y ago
Add your answer:
Earn +20 pts
What has the author David Whittaker written?
David Whittaker has written: 'Stereochemistry and mechanism' -- subject(s): Stereochemistry
What has the author Leo H Sommer written?
Leo H. Sommer has written: 'Stereochemistry, mechanism and silicon'
What has the author William James Hamilton written?
William James Hamilton has written: 'Mechanism and stereochemistry studies in the synthesis and interconversion of oxaziridines and nitrones'
Stereochemistry of hydration in carbon carbon double bond?
In the stereochemistry of hydration of a carbon-carbon double bond, the water molecule can add to either side of the double bond carbon, leading to the formation of two possible stereoisomers: a syn addition, where the hydroxyl and hydrogen groups are on the same side (cis), and an anti addition, where they are on opposite sides (trans). The stereochemistry is governed by the orientation of the reacting groups and the mechanism of the reaction.
What is the mechanism for the synthesis of E and Z alpha phenylcinnamic acid?
The synthesis of E and Z α-phenylcinnamic acid can be achieved through the Wittig reaction, which involves the reaction of an aldehyde or ketone with a phosphonium ylide to form an alkene. By selecting appropriate reactants with specific stereochemistry, either the E or Z isomer can be obtained. Moreover, the stereochemistry of the product can be controlled by the choice of the phosphonium ylide used in the reaction.
What alcohol is synthesized to form 2-Bromopentane?
2-Bromopentane is typically synthesized by reacting 1-pentene with hydrobromic acid (HBr) in the presence of a radical initiator like benzoyl peroxide. This reaction follows an anti-Markovnikov addition mechanism, where the bromine atom is added to the less substituted carbon of the double bond in 1-pentene.
How do you determine the major product on stereo-selective addition reactions?
The major product in a stereo-selective addition reaction is determined by analyzing the stereochemistry of the reactants and the mechanism of the reaction. Factors such as steric hindrance, electronic effects, and the type of reagents used can influence the stereochemistry of the final product. Understanding how these factors affect the reaction can help predict the major stereochemical outcome.
How can reaction be classified?
mechanism. mechanism.
How is a defense mechanism?
What is a defense mechanism
What is the difference between stereoselective and stereoselactive reaction?
In a stereoselective reaction, the reactants can potentially form multiple stereoisomers, but one stereoisomer is favored over the others. In a stereospecific reaction, the reactants can also form multiple stereoisomers, but only one specific stereoisomer is produced.
Fumaric acid with 13- cyclopentadiene gives only one product?
The reaction between fumaric acid and 13-cyclopentadiene forms a Diels-Alder adduct. In this reaction, only one product is formed due to the regioselectivity and stereoselectivity of the Diels-Alder reaction. The reaction proceeds through a concerted mechanism to give a single product with specific stereochemistry.
How can chemical reactions be classified?
mechanism. mechanism.
