85% H3PO4 170 °C ОН

Q: Draw the detailed mechanism and the product for the following reaction. Be sure to include…

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Q: CI CH3OH

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Q: Bonus Question: If you deemed the previous reaction to be unsuccessfull, propose a reaction or…

A: To get the starting molecule we will do the retrosynthetic analysis and by doing this we get toluene…

Q: Synthesis this please. Include reagents that could work and intermediate compound. N

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Step 1 Step 2 Step 3 Step 4 i Draw H3CH2C¯, and then add the curved arrow notation showing a…

A: Nucleophilic reactions are those reactions in which a nucleophile attacks the carbon of carbonyl…

Q: Provide a multi-step synthesis of the target structure on the right from the starting structure on…

A: Here we are required to synthesize the given compound from given alkane

Q: Draw the complete, detailed mechanism for the reaction: conc HCI ?

A: In rection of alkene , at first,  alkene donate electron to H+  and carbocation intermediate is…

Q: Draw the complete, detailed mechanism for the following reaction. 1. ¸MgBr 2. H3O+ (excess)

A: The question is based on the concept of organic synthesis.  we need to synthesize the product using…

Q: c) エ

A: c) The conversion of ethynylbenzene to 2-phenylacetaldehyde. Reagent used: Dilute H2SO4/HgSO4. This…

Q: D July 애 H Drodunt

A: Debromination gives primary carbocation. Now, elimination of proton gives product.

Q: Please draw the major product/products of each of the following reaction

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Q: For each of the following pair of species, which is the stronger nucleophile in acetone? Explain.

A: Given : structure of molecules Tip : less electronegative atoms are strong nucleophile

Q: 1. HBr 2. NaCN, DMSO

A: Markovnikov's rule states that when an asymmetrical reagent is added to an asymmetrical alkene, then…

Q: HI HO х

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Q: In an unsymmetrical epoxide, the nucleophile attacks at the lesssubstituted carbon atom. Explain…

A: In an unsymmetrical epoxide, the nucleophile attacks at the less substituted carbon atom because of…

Q: Draw reaction of an a,b-unsaturated aldehyde or a ketone with a nucleophile forms a direct addition…

A: Given reaction,     a,b-unsaturated aldehyde or a ketone with a nucleophile

Q: Foresee the resulting products from exciting the given molecule and determine which product is…

A: The objective of this question is to predict the resulting products from exciting the given molecule…

Q: NH2 For the reaction shown here, draw the complete, detailed mechanism and major product. 1. CH3I…

A: The expected mechanism and products of the given reaction have been described below.

Q: How can we determine whether the equilibrium will favor products in a nucleophilic substitution?

A: Substitution reaction is a reaction in which an atom or a group of atoms are substituted by either a…

Q: 4. Draw the mechanism of the following reaction.

A: The mechanism for the 1st reaction (Reaction with NH2OH) is shown below:

Q: The reaction shown here proceeds via a carbocation rearrangement. Draw a complete, detailed…

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Q: Draw the major organic product of the following reaction. Inorganic byproducts like water or salts…

A: Organic reactions are those in which organic reactant react to form organic products.

Q: In an SN2 reaction, a lone pair in the of the electrophile. A) o orbital; o orbital B) non-bonding…

A: Substance that tend to donate  lone pair is called nucleophile.

Q: Draw ths missing curved arrow notation for the E2 reaction. AV

A: The secondary and tertiary alkyl halides proceed with E2 mechanism in the presence of base HO- .…

Q: Avobenzone is an active component in many sunscreens. It can exist in an equilibrium between its…

A: a. The keto form of this compound is shown as follows:

Q: Show a possible pathway and include all intermediate and reagents.

A: Dehydration of given alcohol leads to formation of product.

Q: 3. Oxidation of Alcohols Mechanism: Draw the major product for the oxidation reaction below in the…

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