d) но H2SO4 H20 only product! e) H2SO4 H20 MAJOR minor minor

Q: Which of the following mechanisms is drawn correctly? Remember to check arrows, formal charges,…

A: This reaction follows E1cb mechanism i.e, Elimination Unimolecular conjugate base, that first base…

Q: PLEASE SELECT ONLY 1 OPTION FROM THE FOLLOWING ONLY OPTIONS:     Elimination 2nd order Radical…

A: Diels-Alder reaction: The Diels–Alder reaction is a reaction between a conjugated diene and a…

Q: For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer.…

A: Given compound is acyl chloride and it react with grignard reagent. In acyl chloride , there is…

Q: If a trans alkene is reacted with OsO4 in H2S, the product is: Meso compound Hoffman product…

A: Alkene are reactive in nature due to presence of double bond

Q: Which of the following processes could be the termination step in free radical substitution…

A: The termination process for the above free radical substitution reaction is given below

Q: III.

A: The reaction shows [1,5]-sigmatropic rearrangement. Though conjugated double bond there is 1,5-…

Q: In an SNl reaction, among the three given alkyl halides below, [A_ I C[ is expected to

A: It is two step mechanism                     first step is formation of carbocation, it is slow…

Q: For the following reaction, list all expected organic and covalent products. This question does not…

A: The given reaction goes via SN2 mechanism which is a one-step reaction that gives the product with…

Q: The electrophilic addition reaction shown below involves a carbocation rearrangement. HBr For the…

A:

Q: NO2 NaOCH3 CI

A:

Q: Rxn F NaOH

A: The unimolecular nucleophilic substitution reaction (SN1) proceeds in two steps. In the first step,…

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: Complete the mechanism for the formation of the major species at equilibrium for the reaction of…

A: Hemiacetal are formed when aldehyde and alcohol reacts with each other. The carbonyl carbon is…

Q: The following molecules are subject to substitution (SN1 or SN2) reaction conditions. a) Identify if…

A: a) The carbon atom which is attached to 3 more carbon is known as 30 carbon The carbon atom which is…

Q: draw the mechanism and label makor resonance structure catalytic H,50, HO molecule A molecule B

A: This question is asking the basic concept of resonance effect. We know that,  Resonance always…

Q: Q3. For the substitution reactions below, draw out the reactions as shown and answer the following…

A: Inorganic chemistry we learn about two types of substitution reaction. Unimolecular nucleophilic…

Q: FIRST STATEMENT SECOND STATEMENT 47. Chlorination of methyl benzene in UV light proceeds via free…

A: (47) When methyl benzene is treated with Chlorine in UV light then mono, di and tri chloro methyl…

Q: CH, CH, THF/H;0 -: + Hc--CH, CH, + CH, CH, CH Use curved arrows to write the first step of this…

A: Nucleophilic substitution reactions can be defined as the chemical reaction which involves the…

Q: Why do carbocation rearrangements occur? Choose all that apply. Ring strain can be reduced. They…

A: Carbocation rearrangements are the organic reactions in which the movement of an unstable…

Q: a. Addition of HX to alkenes follow Markonikov's rule, forming intermediate. a more stable…

A:

Q: Consider the molecule given below. In theory, there are only two inequivalent hydrogens in this…

A:

Q: Consider the following reaction being performed with a low concentration. Think about what type of…

A: The product of the given reaction is

Q: Please draw all four bonds at chiral centers. Br

A: The product is 2-bromopentane.

Q: PCC -> Predict the Prodyct(s) Of The reacton Include Stereo Chemistry In your answer where relevant

A: PCC is an oxidising agent which oxidise primary alcohol to aldehyde. PCC is pyridinium chloro…

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

A: The given reaction mechanisms are SN1, SN2, E1 and E2 To find: The mechanisms which involves…

Q: Determine whether a 1,2-hydride shift is favorable for the following carbocation. If no…

A: Carbon having positive charge on it is called carbocation The order of stability of carbocations is…

Q: For the substitution reactions below, draw out the reactions as shown and answer the following…

A: This is an Aliphatic nucleophilic substitution mechanism-based question. Find the complete solution…

Q: Using Curved Arrow Formalism, draw the reaction of 1-methylcyclopentanol treated with aqueous…

A:

Q: Br2 undergoes electrophilic addition to maleic anhydride as shown here. Explain why this reaction is…

A: Here in this compound the C=C double bond is resonance stabilized by two keto group adjacent to…

Q: The following condition favors SN2 mechanism for a secondary alkyl halide.

A: We have given that  The following condition favors SN2 mechanism for a secondary alkyl halide.   a.…

Q: Determine the position that is most likely to be the site of an EAS reaction in the compound below:…

A:

Q: In the formal SN1 mechanism, the reaction has two steps; however, in reality ____________ steps are…

A:

Q: For each pair of reactants (A-C) draw all possible E2 products, label each as a mono, di, tri, or…

A: When an alkyl halide reacts with a strong base, the reactants can undergo two mechanisms. The…

Q: (4B) Carbocation Stability: Rank the following carbocations in order of stability and briefly…

A: Carbocation is species in which carbon bears positive charge.

Q: for the Cl2 addition reaction with 1,2dimethylcyclohexene, draw the most reasonable curved arrow…

A: Cl2 when reacted with alkenes, add to opposite faces of the double bond, that is in an anti-addition…

Q: CH2=CH-CH2-CH3 + H2O CH3-CHOH-CH2-CH3 HC C-CH2 CH3 → CH2=CH-CH2-CH3 + H2 HỌ CH + HOCI H.

A: An addition reaction occurs when two or more reactants combine to form a single product. This…

Q: In much the same way that they react with H2, alkenes also react with D2 (deuterium is an isotope of…

A: Given reaction is reduction of alkene .

Q: Complete the mechanism of hydration of alkene below. Please follow curved arrows to predict the…

A: Answer:- The hydration of alkene gives the corresponding alcohol according to Markovnikov rule which…

Q: In the given condensed formula, I understand that there will be a carbocation rearrangement due to…

A: The E1 mechanism of conversion of secondary alcohol to alkene is given in step two.

Q: Q2. Draw the structures for the diene and dienophile you would use to synthesize each of the…

A: As per the name diene is a molecule with alternate double bonds. And the dienophile is the molecule…

Q: Consider the following statement  in reference to SN1, SN2, E1, and E2 reactions of haloalkanes. To…

A: SOLUTION: Step 1: The SN1 mechanism involves the attack of nucleophile from both the sides (above…

Q: Modify the given carbon skeleton to draw the major product(s). If a racemic mixture of enantiomers…

A: We have to draw the products of the given reaction.

Q: Determine the position that is most likely to be the site of an EAS reaction in the compound below:…

A: The compound given is,

Q: Which of the following alkene addition reactions occur/s specifically in syn fashion?…

A: If we say a reactions occur/s specifically in syn fashion, the adding atoms should be on same side.…

Q: Use Hammond's postulate to determine which alkene in each pair would be expected to form a…

A: Answer: According to hammond's postulate, structure of the transition state is more similar to…

Q: Predict the product or starting material of the following alkene addition reactions. Remember,…

A: According to Markovnikov's rule, during the addition of hydrogen halide to unsymmetrical alkene, the…

Q: why does this carbocation go through rearrangemnt by a hydride shift?

A:

Q: Classify the following carbocations as primary, secondary, tertiary, methyl, or vinyl carbocations…

A: We have to predict the type of carbocation.

Q: Describe all of the reasons why first-order substitution and elimination reactions can produce a…

A: In this question, we will discuss about why first order reaction ( for both Substitution and…