Using curved arrows show the mechanism for the following reaction

Q: OH 1. LIAIH4, THF OCH2CH3 2. H3O* HOCH,CH3

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Q: 2) Show an acceptable mechanism for the following transformation using proper curved arrows. HO

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Q: Show the mechanism (arrow pushing) for the following reaction: 1. NANH2 2. Br

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Q: Show the product of the following reaction. nucleophilic carbene catalyst

A: The terminal alkenes present at C-13 and C-1 on the same molecule, leading to an intramolecular…

Q: Using lithium enolate with ester and alkyl halide, draw the reactants and steps of the reaction that…

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Q: Show the complete mechanism for an E2 reaction with 1-bromo-2-tert-butylcyclohexane

A: In this question, we will draw Complete mechanism for E2 Reaction.  You can see details Solution…

Q: show the steps for synthesis of the product using the given starting material.

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Q: Draw curved arrows to show the movement of electrons in this step of the mechanism.

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Q: ? Но

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Q: Write a mechanism for the step shown below, using curved arrows to show electron redistribution.…

A: In acidic medium, oxygen of substrate takes the proton of acid. And if already oxygen is protonated…

Q: Draw the curved mechanism arrows that show the deprotonation of phenol by NaOH and draw the major…

A: This the acid base reaction where NaOH act as  strong base and Phenol acts as a slightly milder…

Q: The correct product of this reaction is

A: Since we know that additional of HBr to alkene take place by ionic Electrophilic addition reaction .…

Q: Complete the mechanism for the reaction of butanone with NABH, followed by the addition of aqueous…

A: When a ketone is reduced with sodium borohydride and acidic hydrolysis, then ketone is changed into…

Q: Give the major product of the reaction

A: Given reaction follows sn2 mechanism.

Q: Show a mechanism for how the product is formed. Your mechanism must use curved arrows to represent…

A: Given : organic reaction.  Here elimination is occuring, since weak base H2O is given, E1 reaction…

Q: Explain the strength of the base usually determines whether a reaction follows the E1 or E2…

A: Elimination reaction is the reaction in which small molecule like water, ammonia are eliminated.…

Q: For the following reaction, draw the correct product that you would expect to form under Robinson…

A: Given - Product = ?

Q: Please show the complete steps as well as arrowing pushing mechanisms for the following reaction.

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Q: Draw the mechanisms using curved arrows and predict the product for the reactions.

A: When electrophile is added to the conjugated diene, two types of products are possible, kinetic…

Q: Using the Strecker Reaction, please show the steps and the final product of the following reaction:

A: Strecker synthesis is preparation of alpha- aminonitriles which are intermediate for the synthesis…

Q: Give the major product for the following reaction

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Q: Show a detailed mechanism (using arrows) for the nucleophilic substitution reaction that would take…

A: Show a detailed mechanism (using arrows) for the nucleophilic substitution reaction that would take…

Q: B. Using curved arrows, show the mechanism for the formation of A-1 haloalkane through electrophilic…

A: Formation of haloalkane:

Q: Which types of halide will react faster in an SN1 reaction?

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Q: Show a mechanism for how the product is formed. Your mechanism must use curved arrows to represent…

A: Given : reaction It is an elimination reaction, since strong base is given so it is E2 elimination.

Q: Please write the mechanism for the following reaction.

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Q: Draw the mechanism for each of the following reaction. Show all steps in the reaction, the…

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Q: down the product

A: Given:

Q: Show two different ways to make an epoxide from a trans alkene, one that gives the trans epoxide and…

A: Trans product :

Q: Show all the arrow mechanism including the PROPER reagents.

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Q: Draw curved fishhook arrows to show the movement of electrons in this step of the reaction…

A: In a free radical reaction mechanism, the homolytic bond cleavage takes place. During homolytic bond…

Q: Propose this mechanism

A: Given reaction,

Q: а.) b.) с.)

A: Acetals on hydrolysis gives corresponding aldehyde or ketone and alcohols. Let's see here,

Q: Give a mechanism for the following reaction.

A: We have to predict the mechanism.

Q: HONH, CI- , NaOH

A: This is an example of condensation reaction in which hydroxylamine condensed with 1,3-dikketone to…

Q: acid anhydride alcohol

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Q: For each reaction below, show mechanism including curved arrows

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Q: Meo ACOH MeO. NH2 NH

A: This is two step process. First step is the acid catalyzed imination of amine with aldehyde. second…

Q: Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing…

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Q: H

A: Applying concept of organic synthesis via wittig reaction and organometallic.

Q: Na HO, Br

A: When an alcohol is treated with NaOH, the following acid-base equilibrium occurs.   The…

Q: Show the retrosynthesis mechanism of this equation with curved arrows representing electron transfer…

A: Note : 1-Butene on hydroboration and oxidation produces the 1-butanol. Benzoic acid and 1-butanol…

Q: Choose the reagent(s) that would be most likely to complete this reaction.

A: Given: reaction of formation of 2-pentanol from pentene. To find: suitable reagent for this…

Q: Show the mechanism for the following reaction

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Q: Draw the structure of the product of the following reactions.

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Q: Use curved arrows to show the movement of electrons in the attached E2 mechanism. Draw the structure…

A: E2 mechanism:- E2 refers to the elimination reaction which having bimolecular rate of reaction. In…

Q: „coH COH

A: ANSWER > This is a radical reaction .In radical reaction the weaker the C-H bond, more readily…

UV Visible Spectroscopy

Spectroscopy refers to the absorption or emission of light or other radiations by matter. When a substance or chemical absorbs light or radiation, they reach an excited state followed by de-excitation or emission of the light or radiation forming distinct spectra. UV-visible spectroscopy or  ultraviolet-visible refers to the absorption and emission in the ultraviolet and visible regions of the electromagnetic spectrum.