1. LDA Ph 2. PHCH2B1

Q: Write the complete mechanism with arrows of the following reaction. A

A: This reaction is a [1,3] cycloadditon reaction.The mechanism is as given below.

Q: Give the major organic product(s) for each step of the following reaction

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

Q: Examine Solved Problem 7.3. Your task is to prepare A in the highest possible yield by…

A: Interpretation: To prepare A i.e 2-methyl-1-butene by dehydrobromination in highest possible yield…

Q: explain the presence of trans-9-(2-phenylethenyl anthracene) by wittig reaction. detail description…

A:

Q: The activating and deactivating groups could affect the position(s) of the next incoming group(s) to…

A: Activating groups: ortho or para directors Substituents on the ring are groups that donate…

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: Q2. What are elimination reactions? Illustrate and describe the E2 reaction mechanism. Compare and…

A: Important types of organic reactions are Addition reaction, elimination reaction and substitution…

Q: Complete the following transformation and provide the detailed steps

A: Aldehyde is protected using a protecting group and another aldehydic group is reduced to alcohol…

Q: Propose

A: When alcohol is heated then water molecule gets eliminate and we get alkene.

Q: a) Describe the general steps in the mechanism for an SN1 reaction and an SN2 reaction. b) Discuss…

A: The reaction in which an atom or group is substitutes by any other atom or group is known as…

Q: Explain the mechin CHs NO2 SbFs HF -> in Toulene No2 over 95.

A: At first SbF5 reacts with HF to give SbF6^- and H^+.  This H^+ is attacked by nucleophilic NO2…

Q: Give a complete mechanism with step by step in details OMSO I10'c

A: In this question, we will draw the reaction mechanism step by step with details. You can see below…

Q: Show the mechanism and products formed when the given molecule reacts with NaOD and D2O.

A: When D2O is added in the reaction, the deuterium atom substitutes the proton of hydroxyl group. The…

Q: Provide

A: Tertiary alkyl halide in polar protic solvent undergoes alkene.

Q: Define mechanism Acid-Catalyzed Halogenation at the α Carbon ?

A: Applying concept of organic synthesis.

Q: In both examples below the reactants shown are combined to bring about a nucleophilic substitution…

A: If weak base is used (dil.NaOH), substitution reaction takesplace  Benzyl chloride undergo SN1…

Q: Br2 / N2OH R-CO-NH2 R-NH2 H20

A:

Q: heel HO он NaOH (a)

A:

Q: (iii) PPH3 + Mel NaH >?

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

Q: illustrate detailed mechanisms to complete the reaction

A: Alcohol reacts with HBr gives a rearranged product. Intermediate is carbocation, hence carbocation…

Q: The phenyl group, C6H5, is known to be an ortho/para-directing group. (a) With that in mind, predict…

A: Firstly, one thing to remember is that all the ortho/ para directing groups has one pair of…

Q: on the right. You do NOT need to show the mechanisms for the rea но он 18.

A: Answer

Q: Problem attached

A: The organic reactions are carried out with the help of specific reagents. Every reaction is guided…

Q: 3. Rank the following in order by the rate in which they could participate in an SN1 reaction (“1"…

A:

Q: provide the mechanism and reagents to perform the reaction. Br Но

A: To provide the mechanism and reagents for the given reaction

Q: How Reactivity Depends on the Basicity of the Leaving Group?

A: Applying basic concepts of relationship between  leaving ability and base character of leaving…

Q: Please write the full mechanism of the following reaction

A:

Q: Give clear handwritten solution) give reaction mechanism and major product for the all three…

A: The Given question is various types Of bromination Reaction.

Q: 5) Provide a complete and detailed mechanism for these transformations. OH heat, acid +

A: We have to predict the mechanism for given reaction.

Q: a) ОН ОН b) CI HO

A: Here we have to prepare the following compounds from the given starting material in multistep…

Q: Suggest a reasonable mechanism for the following reaction Ph OCH3 Ph. OCH3 FeCla Ph Ph OCH3

A: FeCl3 acts as a catalyst. It helps in removal of methoxy group to produce electrophile. Attack of…

Q: to

A: This synthesis involves Michael addition, Aldol condensation, dehydration, hydrolysis and…

Q: a) What is (are) the major product(s) of the nitration reaction. Explain this selectivity, and…

A:

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: 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: Complete the following reaction and provide a detailed, step-by-step mechanism for the process. HBr

A: It is an SN1 reaction. This reaction based on a more stable carbocation intermediate. First, alkene…

Q: Write in details the explanation of this mechanism, from the beginning till the our product B-ione.…

A:

Q: provide a mechanism for this

A: Given reaction is a example of E2 reaction .This is a one step reaction in which Hydrogen is removed…

Q: Question attached

A: Complete the following reaction and provide the reaction mechanism

Q: Complete and detailed n-butyl bromide synthesis mechanism.

A:

Q: O Complete the following reaction and provide a detailed, step-by-step mechanism for the process.…

A:

Q: ZEU-UEU-UEZ

A: The Diels–Alder reaction is a chemical reaction that occurs when a conjugated diene reacts with a…

Q: Provide the product of this reaction. Assume only mono-substitution takes place. Hint: Consider the…

A: Mono substitution:

Q: Complete the following reaction and provide a detailed, step-by-step mechanism for the process. !…

A: Hydration of alkene: Alkene gives hydration reactions in presence of an acid catalyst. In this…

Q: Base Compound 2 Compound 1 B.

A:

Q: Provide a plausible arrow pushing mechanism for the reaction below. You may abbreviate the…

A: The plausible arrow pushing reaction mechanism is provided below in attach image .

Q: Provide the major organic product in the reaction shown below.

A:

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.