write one name reaction with mechanism . Give four example of this name reaction with mechanism of each four . ( please dont miss mechanism, do as given in question i will surely upvote ) write clearly in white paper . Thank you

Q: NaOEt ELOH elimination product 8. Br

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Q: NH₂

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Q: using the picture create a detailed mechanism for terminal alkyne

A: It is the conversion of 1-hexyne to hexanal in presence of BH3 and H2O2/OH-. The overall reaction…

Q: Nucleophilic attack may appear to occur in two steps as shown below. The alcohol is the nucleophile…

A: The carbon atom double bonded to oxygen atom and single bonded to two alkyl groups is called…

Q: ОН

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Q: could somebody help me explain why the first product is major and the second one is minor please?…

A: Okay I will explain you in details why first Product is major but second Product is minor product in…

Q: Explain why A cross couples with the aryl iodide, rather than two molecules of A coupling together…

A: Aryl coupling is commonly a cross-coupling reaction. That means the reaction starts when two…

Q: For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be…

A: We know that SN1, E1 and SN2, E2 mechanisms follow the first and second order kinetics respectively.

Q: Does dehydrogenation of alkyl halides create Zaitsef or Hoffman products? In this example, which is…

A: Alkyl halide undergoes dehydrogenation reaction in presence of a base and form alkene. This kind of…

Q: I need a detailed reaction mechanism of this synthesis

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Q: I’m struggling to find the steps for the product. Can you elaborate them?

A: Applying concept of reagents and name reaction.

Q: Q. Can anyone please show me the details steps involved in the retrosynthesis of the target…

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Q: (a) Consider the reaction below, and answer the questions that follow: UV ight (i) Draw a curved…

A: The reaction sequence given in the question represents a uv mediated ring closing reaction of a…

Q: Explain how a student will able to isolate the mono eliminated product in good selectivity used in…

A: products are seperated on the basis of their physical properties.

Q: Write a detailed mechanism f

A: Protonation of alkene  Attack of alkene as nucleophile (intermolecular reaction)   Deprotonation

Q: Give the reagents and results/observation

A: NaHSO3 test : This is a characteristic test for carbonyl compounds. This test is given by small…

Q: For the reaction below provide all possible product(s) and circle the major product.

A: This reaction is Aldol Condensation reaction in the presence of acid water. You can see details…

Q: b) A key piece in the synthesis is the molecule below. Provide a reaction that makes this piece that…

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Q: draw the curly arrow mechanism for this experiment, include all details like electrons, curly…

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Q: Please clearly draw the overall reaction taking place between methyl salicylate and sodium…

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Q: While we are at it, let's do the same thing for the second step of the mechanism. Again, what is…

A: Answer

Q: kindly answer a and b, asap. Thank you!

A: The structure of the given compound is :

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: Cyanohydrin formation is useful because of the further chemistry that can be carried out on

A: C=O group is called carbonyl group  Aldehyde and ketone both are combinedly called carbonyl…

Q: Complete the mechanism for the given Stork enamine reaction by drawing curved arrows, atoms, bonds,…

A: Carbonyl compounds react with a secondary amine to form an enamine. Enamines are nitrogen analogous…

Q: Show any reaction that attaches one or two deuterium atom(s) selectively on carbon.

A: Deuterium is an isotope of hydrogen. It is a double standard gas as it has two atoms in one atom. It…

Q: Shown below are two reactions; Reaction 1 is a Friedel-Crafts acylation while Reaction 2 is a…

A: Friedal crafts acylation and alkylation both are electrophilic aromatic substitution reaction.

Q: + HA Please write the mechanism arrows for it as an Sn1 mechanism please

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Q: H. H. CH3 CH,0 CH3 Sx2E2 CH3

A: It is an example of bimolecular nucleophilic substitution.

Q: This is a retro synthetic analysis problem, shown here is the final product (initial material is…

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Q: When an epoxide is placed in aqueous acid, the ring opens and a diol forms. Below is the ring…

A: In acid catalysed ring opening reaction ring opening takes place  from more substituted side.

Q: For this question, would both of these products be anti-Markovnikov products? I'm confused why the…

A: If in this reaction, you will taking HCl with peroxide for anti-Markovnikov reaction then first…

Q: write one name reaction with mechanism . Give four example of this name reaction with mechanism of…

A: It is a rearrangement reaction. This reaction is [3,3] sigmatropic reaction. It is rearrangement of…

Q: For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be…

A: The given options are : a). SN1 = Unimolecular nucleophilic substitution reaction. b). SN2 =…

Q: Analyze the reaction below, and determine the reagents necessary to carry out the conversion. Be…

A: Given reaction is example of chlorination reaction.  Chlorination of tertiary butyl benzene is…

Q: Propose a curved arrow mechanism for ma making this product: H

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

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Q: For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be…

A: An organic reaction in which a reactant molecule, containing a good leaving group, reactant with an…

Q: Native chemical ligation works by sequential nucleophilic acyl substitution reactions, but the…

A: In nucleophilic acyl substitution reaction, the nucleophile attacks the electron deficient carbonyl…

Q: A problem in dyeing fabrics is the degree of fastness of the dye to the fabric. Many of the early…

A: When a nucleophile displaces a leaving group from an aromatic system, then the reaction is termed as…

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: Using curved arrows to show the flow of electrons, and being careful to balance mass and charge for…

A: Given : reaction

Q: Knowing the properties of organic molecules, students will now design experimental set-ups that will…

A: Here a scheme for the organic synthesis of an important organic molecule is given. There are 3 steps…

Q: b) T.

A: The question is based on the concept of organic reactions. We have to identify the reagents used in…

Q: ? CH, Hint Remember that overalkylation is a problem when it comes to Friedel-Crafts

A: Friedel-Crafts alkylation is the process of replacement of an aromatic proton by an alkyl group and…

Q: NO2

A: The organic reaction takes place in many steps. These steps involve the use of various reagents.

Q: break down of this reaction in sequence and a complete reaction scheme

A: In the given reaction ferrocene is reacting with acetic anhydride in the presence of H3PO4 to…

Q: CN

A: The conversion involves reaction of aldehyde with grignard reagent followed by substitution 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.