NaOMeOMeandMeOHBrrefluxYou are trying to maximize the yield of the alkene product, but are still getting a decent amount ofthe substitution product in the current reaction conditions. How might you increase the selectivitytowards the alkene product? Hint: the word reflux is important here.Turn the hot plate up. In other words, increase the heat output on the hotplate to elevate the reactiontemperature.Run the reaction at room temperature, rather than at reflux.Run the reaction in a sealed tube in a microwave reactor. You can increase the temperature beyond the boilingpoint of the solvent.Run the reaction in an ice bath.

The alkene product is an elimination product. To increase the selectivity of alkene product over…

NaOMe OMe and MeOH Br reflux bu are trying to maximize the yield of the alkene product, but are still getting a decent amount of e substitution product in the current reaction conditions. How might you increase the selectivity wards the alkene product? Hint: the word reflux is important here. O Turn the hot plate up. In other words, increase the heat output on the hotplate to elevate the reaction temperature. O Run the reaction at room temperature, rather than at reflux. O Run the reaction in a sealed tube in a microwave reactor. You can increase the temperature beyond the boiling point of the solvent. O Run the roa in an ie bath

NaOMe OMe and MeOH Br reflux bu are trying to maximize the yield of the alkene product, but are still getting a decent amount of e substitution product in the current reaction conditions. How might you increase the selectivity wards the alkene product? Hint: the word reflux is important here. O Turn the hot plate up. In other words, increase the heat output on the hotplate to elevate the reaction temperature. O Run the reaction at room temperature, rather than at reflux. O Run the reaction in a sealed tube in a microwave reactor. You can increase the temperature beyond the boiling point of the solvent. O Run the roa in an ie bath

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter8: Addition Via Carbocation

Section: Chapter Questions

Problem 18CTQ: The reactants, intermediates, final products, and all curved arrows showing bonds forming...

See similar textbooks

Similar questions

Fill in the missing starting material, reagant, or product where neccessary.
HELP ASAP! please write out mechanism and reagants/reactants for this
1 example of reaction for each of the types of organic reactions: substitution, elimination, addition, and rearrangement. Show:a. the overall reaction (reactants --> products)b. the reaction mechanism (indicate intermediate product)c. indicate which is the reactive species or intermediate in the reaction (radical? electrophile? nucleophile?)d. overall description of the reaction eg., radical substitution or SR
The quick rule which allows prediction of the major product for electrophilicaddition reactions to alkenes (such as shown in question 2) works mechanisticallybecause the electrophile adds to theC=C in the directionthat forms the (a) least stable carbocation, (b) most reactive nucleophile, (c) moststable carbocation,(d) lowest classification of halide.
I understand what reagents and or solvents can be used to get from an alkene to an alkyne but if someone could please show me step by step how each is used to perform the actual synthesis? Like how does each thing work to get to the next portion of the synthesis. I am truly struggling. thank you
The reactants, intermediates, final products, and all curved arrows showing bonds forming andbreaking are collectively referred to as the mechanism of a reaction. For the following reactants: a. Explain why the original statement of Markovnikov’s rule does not help in this case, but themodern restatement of Markovnikov’s rule tells you which carbon will get the X (Cl). b. Show the mechanism of the most likely addition reaction between the reactants.
I need help explaing how the mechanism works step by step and also shpwing it please from this lab
Please show the mechanism and the reactant. thank you
Chemistry please provide the flow of electrons aswell!! thank you! using the starting material (on the left) to determine the sythetic route which will be the most reaosnable and effective to theres none, you have to start witth the begin products to get to finish needed by using the minmium reagents and reactions needed to get to the final product
How is this incorrect and what is the correct mechanism?
Identify the HOMO and LUMO in the first step of the reaction shown here:
About: Substitution vs. Elimination Reactions Note: Identify the major and minor product (s) that are expected for each of the following reactions.