Provide a complete curved-arrow mechanism for this transformation

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

A:

Q: With an example describe mechanistically how an extraction is carried out acid-base.

A: Acid-base extraction is employed to separate acidic and basic compounds from a mixture.

Q: OCH3 FeBr3 , Br2 OCH3 Br

A:

Q: Draw a detailed, arrow-pushing mechanism for the conversion of benzoic acid to methyl benzoate under…

A: We have reaction of benzoic acid and methanol to form the methyl benzoate in acidic conditions. We…

Q: Show, using the curved arrow notation, the mechanism of alcohol dehydration of 2-methylcyclohexanol…

A: Dehydration  process is process where loss of water take place

Q: Could you help provide a complete curved arrow mechanism for this transformation?

A:

Q: Is the crude (non-crystallized) acetanilide pure? Why or why not?  Is the crystallized acetanilide…

A: Any crude compound like acetanilide can't be ultra pure . Because it contain lots of impurities…

Q: Give the mechanasim Br₂ ccty HBr H₂02 НВО C

A: Reaction 1 : Br2 addition to alkenes produces trans -1,2-dibromo compound. Reaction 2 : HBr addition…

Q: 2. Explain why tert-butyl chloride will undergo an Sw1 but not an Sw2 reaction process?

A:

Q: Write a mechanism for the following reaction

A: The details solution for this is provided below in attach image.

Q: Perform a retrosynthetic analysis and suggest a synthesis of the target molecule (on the left) from…

A: The Retrosynthesis method is the method that determines the starting material by the fragmentation…

Q: Please

A: We will write all the intermidiate

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

A: E2 mechanism is a concerted mechanism.

Q: Show the electron-flow mechanism of the synthetic schemes (Aniline) of the picture below. This…

A:

Q: Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Long and detailed explanations…

A: The absolute configuration at two stereogenic centres of the newly discovered drug can be identified…

Q: Please show the complete process and mechanisms for 1, 2 and 3 (in picture): P.S. Please write in…

A: 1) In first case base will abstract the acidic hydrogen form acetylene and form the salt which was…

Q: -) Give reagents and conditions that will allow ALL of the following synthetic transformations to be…

A: 1) Hydroboration oxidation of alcohol is used for Anti-Markovnikov addition of water to an alkene.…

Q: Predict the mechanism of the rection below.

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: For each pair of compounds, a state which compound is the better SN2 substrate. (a) 2-bromobutane or…

A: Reactions in which leaving group is readily replaced by an incoming nucleophile is called…

Q: show the conversion of 2-chloro-2-methylbutane to 2-methyl-2-butene and 2-methyl-1-butene, with a…

A:

Q: Complete the mechanism for the following mixed Claisen condensation by adding any missing atoms,…

A:

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

A: E2 mechanism is a concerted mechanism.

Q: O, N. Na OHCag) + Nacl

A: Acid-Base reaction:  In chemistry acid-base reaction is the fastest reaction and salt will be formed…

Q: Show how you would accomplish the following synthetic conversions. More than one step be required.

A: In the above reaction, alkane is being converted to alcohol.

Q: What simple characterization techniques can you say that your product is dibenzalacetone?

A: Characterization techniques are the methods to identify, analyze the chemical substance and…

Q: Do a retrosynthetic analysis on the following compound, ending withavailable starting material.

A: Unconjugated dienes have the double bonds separated by two or more single bonds. They are usually…

Q: How can this transformation be carried out using only heat or light?

A: Given, The ring opened compound formed in the first step has three conjugated pi bonds involved in…

Q: (a) Propose a reasonable mechanism for the following transformation. Use curved arrows to clearly…

A: 1. Intermediates are like Carbocation, Carbanion, free radical ect.  2. Transition state is the…

Q: Part A (1 of 1) Draw the curved arrows for Step 2 of this mechanism. Arrow-pushing Instructions…

A:

Q: Do a retrosynthetic analysis on the following compound, ending with the given starting material:

A: Reterosynthesis is a hypothetical imagination to identify the starting materials to synthesize the…

Q: Determine the number of stereogenic centers in the compound below.

A:

Q: Based from your basic knowledge about GC, do you need to perform derivatization technique prior to…

A: Gas chromatography is a analytical technique used to separating and analysing compounds.GC is used…

Q: stereogenic centers

A:

Q: Why do we need to allow the solution of KF reagent to stand overnight before standardizing? if…

A: Answer : KF solution is stored overnight before standardization to reduce its reactivity. It is…

Q: Draw a detailed mechanism, showing appropriate bonds forming and breaking, for the reaction between…

A: The given reactants, cyclopentadiene and methyl acrylate undergo a Diels-Alder reaction, which…

Q: Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Which compound below undergoes…

A: Alkenes undergo addition reaction with HBr to form alkyl halide. The H+of HBr acts as an…

Q: Part A (1 of 2) Draw the curved arrows for Step 2 of this mechanism. Arrow-pushing Instructions H…

A: In a chemical reaction; the substance which involves in conversion is said to be reactant whereas…

Q: Provide the retrosynthetic analysis and synthetic route for the following Compound.

A:

Q: Explain why compound A will not undergo a ring-opening reaction under thermal conditions, but…

A:

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

A: The movement of electrons in the following E2 mechanism has to be shown The structure of the…

Q: The following transformation is

A: The convertion of alkene to alkane can be done by hydrogenation of carbon carbon double bonds. The…

Q: Draw a reasonable mechanism for this reaction. Interactive 3D display mode Ph Ph-P=CH, CH2 Ph

A:

Q: menthol он он OH OH HO, A в D E

A:

Q: By giving the reagent and the visible result, differentiate each of the following pairs

A: NOTE: please note according to our policy , we can only answer first three subparts of a question.…

Q: Determine whether the sollowing are SN1,SN2, E1, or E2 and draw the major product and if more than…

A:

Q: Thiatriazoles, when heated de-compose vigorously. Why is this?

A: On heating thiatriazoles decomposes to form nitogen gas and isothiocyanate. Because nitrogen is a…

Q: Show and label the mechanism for the SN1 reaction using the generic chemical species and electron…

A: SN1 is called as unim nucleophile substitution reaction. This reaction takes place in two steps…

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: Aldol Condensation- Synthesis of Dibenzalacetone The protocol says that, after adding in all the…

A: Stirring the reaction mixture speeds up the reaction rate. The speed of stirring also matters…

Q: please help with this question. thank you. Propose a mechanism for this transformation

A: We have given the organic reaction we have to find the major product of reaction.

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.