NH2 + H2O2 ية o=s 1 NH₂ 98% H2SO4 50-55 °C OUSMO HO-S 2 NH2 NH2

Q: What are the products for each of these? What's the whole mechanism for B?

A:

Q: The

A: Alkyl halide and alkoxy both react  and gives ether via SN2 mechanism.

Q: What is the reaction mechanism (with arrows) of the following reaction?

A: The objective of the question is to predict and elucidate the detailed reaction mechanism involved…

Q: Predict the reactants and draw the energy diagram that shows the transition state of the reactants:…

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Q: Determine the reagents that would yield the product. Show the intermediates. OH Br

A: Here we are required to find the reagent needed for conversion of ethyl benzene to desired product

Q: Match the following Sulfur containing Functional Groups to its General Structure R1-S N-R3 A.…

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Q: desired product actual product 1. LDA, -78 °C 2. CH3BR Explanation: HO 3-Br/ HO. CH3

A: In the given reaction, LDA (Lithium Diisopropylamide) acts as a strong base and abstracts the most…

Q: Which is the energy required to reach the transition state of an organic reaction? Select the…

A: The transition state is unstable. Therefore molecules of reactant quickly proceed to the next step…

Q: Propose

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

Q: НО. H3O+

A: Product of following reaction can be made by applying appropriate reaction mechanism.

Q: -OH H2O what is the mechanism for the reaction with the product

A:

Q: a similar fashion, draw intermediate 1 and intermediate 2 (final product) for the following reaction

A: Given is organic reaction. The given reaction is bromination reaction. This is an electrophilic…

Q: The following reactions are labeled according to the mechanism by which they proceed. Choose those…

A: Answer is explained below.

Q: Draw the mechanism and the energy diagram for the reaction shown below. Include any resonance…

A: The acidic hydrolysis of di-substituted alkyne produces a ketone.

Q: Predict the products of this organic reaction: CH3 O CH3−O−CH—C—OH + NaOH Δ No reaction ?…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Write a mechanism for this reaction: Br Br2 H₂O + OH Br он

A: Alkene reacts with bromine and water to form beta bromo alcohol. The reaction follows the…

Q: What reaction category/mechanism type does the following reaction fit? O addition substitution (SN1)…

A: SN1 reactionIt is a two step nucleophilic substitution reaction in alkyl halides.The rate is…

Q: но H,CO

A: Since you have posted multiple questions in a single session we are entitiled to answer first…

Q: 4) Write the structure of the organic compound that gives these products on ozonolysis: O3 CO, + HO…

A: Given

Q: Draw the reaction mechanism and the major organic product(s). HI C- CI NH + + CH₂OH Br methanol…

A:

Q: What are the 2 different mechanisms of bromination reactions? What hydrocarbons undergo these…

A: The formation of the RX compound, in which R represents an alkyl group and X represents a halogen…

Q: Identify the product for this reaction. N /Rd.C 1am/25°C

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Q: Predict the correct structure of the product for the given reaction CH HBr

A: The correct structure of product of above reaction is given in attached image.

Q: Consider the reaction - predict the most likely PATH (singular) based on the reactants provided, and…

A: Nucleophilic substitution reactions are reactions in which a nucleophile replaces a leaving group.…

Q: N(CH3)2 HO,

A: The given compound is a secondary alcohol. Here we have to convert the given compound to the given…

Q: Draw the PRODUCTS of the reaction and draw the COMPLETE MECHANISM of the reaction.

A:

Q: explain the mechanism for the electrophilic addition for alkynes

A: Alkyne gives an electrophilic addition reaction with hydrogen halide. The reaction proceeds in two…

Q: What are the organic products of these reactions? Are they electrophiles or nucleophiles? What is…

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Q: CI CN NaCN H3C CH3 H3C CH3

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Q: Answer the question below the reaction. ха In the first step of the reaction mechanism, which of the…

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Q: Select the major intermediate in the chlorination (Cl2/AlCl3) of benzoic acid. COOH бас -CI COOH A…

A: Here AlCl3 is an lewis acid.It helps to increase electrophilicity of chlorine molecule.

Q: Br Br Nal, acetone "H. CH3 H"

A: This reaction is an elimination reaction. It is known as dehydrohalogenation reaction which results…

Q: Draw the reaction mechanism between ethane and chlorine in the presence of light step-by-step and…

A: The ethane and chlorine react in the presence of light to form ethyl chloride as major product.

Q: What reducing agents should be used to obtain the desired target molecules?

A: The catalytic hydrogenation of but-2-enal in the presence of palladium catalyst forms butanal…

Q: The conversion of (CH3)3CI to (CH3)2C=CH2 can occur by either a onestepor a two-step mechanism, as…

A: The mechanism of reaction (2) follows E1 elimination:

Q: What Reaction mechanism is used to make trichloroethanoic acid, CCl3COOH from chlorine and ethanoic…

A:

Q: Explain why this reaction is not possible

A: In elimination reaction the olefins are formed. Elimination reaction are two types E1 and E2.  If…

Q: Tell which of these transformations are oxidations and which are reductions based on whether there…

A:

Q: N-R - NaOH(aq), A RNH₂

A: Hydrolysis is a chemical reaction that involves the breaking of a chemical bond in a molecule with…

Q: Consider the attached SN2 reaction. Question: What happens to the reaction rate in each of the…

A: SN2 is biomolecular nucleophilic substitution reaction. The reaction takes place in single step.…

Q: Question 5: Draw the two routes to create the following alkene by a Wittig reaction and identify the…

A: In the given question we need to find the routes or reactants from which the given alkene can be…