Draw all the posside constitutional isomers for the molecular formula C HaCI. Rank them acording in Sya reactions. to reactivity Slowest Rxn Fastest Rxn

Q: fallowing What are theproducts reactions. Draw mechanis.m. and specify their stereachemistry- fthe…

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

Q: Solve this

A: A rearrangement reaction is a broad class of organic reactions where the carbon skeleton of a…

Q: Draw the mjor product of both question with mechanism asap

A: Given structure of reactants.

Q: e) Rate of SN2 reaction depend on the concentration of both nucleophile and alkylhalide while SNl…

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Q: OMe Br H,N

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Q: nsider the reaction. H :çi: H CH3 H-ci: H3C--C-CH3 H3C CH3 ČH3 dd curved arrows for the first step.…

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Q: TH.

A: Given images are : Increasing order of rate of nucleophilic addition = ?

Q: Br H-Br

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Q: (SYN) Which solvent-acetone or tert-butyl alcohol-would be better to use to carry out the reaction…

A: E1 reaction is a unimolecular elimination reaction, which involves the removal of an HX substituent…

Q: Which following react faster in in an Sn1 reaction,cis-1-bromo-4-tert- butylcyclohexane or…

A: The steric hindrance of huge groups decreases the reaction rate of SN1.

Q: Which EAS reaction is matched with the WRONG electrophile

A: We have been asked which electrophile is wrong for particular Reaction in electrophile aromatic…

Q: tпon of the pгoduct 1опоwing molecule undergoes an intramolесular reaction in shown below. presence…

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Q: Cuven the alchal group is poor leaving group. Explain how reactions with alcohols are carried out…

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Q: a) cuved amow nelation + draw mechanism include stereo, interrediates + final product, include lone…

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Q: CI H30* Choose. ?

A: We have to predict the, product of the given reaction.

Q: no reaction. A diene trand in nakere, it will not undorgo diela aldri reaction.

A: Here we have to determine the starting material required to prepare the given adduct. We can solve…

Q: Draw the missing curved arrow notation to incidate how the carbocation in left box rearranges to the…

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Q: Explain synthetic event in React js

A: SyntheticEvent may be a cross-browser wrapper around browser’s native event. In React all of your…

Q: Rank the nucleophile strength of the compounds below from weakest to strongest

A: A nucleophile is defined as a chemical species that can donate its electron pair. So, it is cleared…

Q: Draw ths missing curved arrow notation for the E2 reaction. AV

A: The secondary and tertiary alkyl halides proceed with E2 mechanism in the presence of base HO- .…

Q: Alkene A can be isomerized to isocomene, a natural product isolatedfrom goldenrod, by treatment with…

A: The alkene is converted to the desired product i.e. isocomene by the formation of a carbocation…

Q: Draw the free energy diagram for each of the reactions in Problem 8.33. For each diagram, include…

A: E1 E1 is a unimolecular Elimination reaction. Here, the removal of an HX take place, this results in…

Q: Draw a detailed free energy diagram comparing the exergonic Sy2 reactions with methoxide and ethanol…

A: Here we have to draw free energy diagram comparing the exogeneric SN2 reaction with methoxide ion…

Q: Propose a complete mechanism for the following reaction. Be sure to use correct curved arrow…

A: The reaction is Friedel Crafts alkylation reaction. The reaction proceeds via the formation of a…

Q: Which nucleophile gives the highest overall reaction rate in SNl reactions? Select one: O F O cī all…

A: SN1 reaction is unimolecular . It means in the rate determining step , there is only electrophile .…

Q: Draw the reactant(s) for the following reaction.

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Q: Br OOCH3

A: Reaction 1: Secondary alkyl bromide and strong base (methoxide ion) prefers E2 elimination. Reaction…

Q: Determine the major product of each reaction in Problem  and draw the complete, detailed mechanism.…

A: Appropriate mechanism and stereochemistry are given below

Q: When benzyl bromide is treated separately with KI and CH3OH, the substitution products are different…

A: The complete reactions are shown as follows:

Q: che following Elimination reaction mechanism, which steps shows correct use of curved arrows? OTs…

A: The mechanistic pathway of the given reaction can be decided based on the nature of the leaving…

Q: (SYN) A student wants to carry out the reaction shown here. Explain the problem(s) associated with…

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Q: Friefly explain why the following synthetic step is incorrect, and rewrite it so that it is correct.…

A: Need to correct the product for the given reactant.

Q: 1.70 An a,ß-unsaturated ketone reacts with a conjugated Wittig reagent to produce a relatively…

A: The wittig reaction is a chemical reaction for the formation of alkene from aldehyde or ketone with…

Q: (SYN) Show how to carry out each of the following transformations. (a) (b) ? ? (c) (d) ? ? CI HO

A: “Since there are multiple sub-parts in this question and it is not mentioned that which one has to…

Q: CHO AcD cl

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Q: alkyl halde The mechanism of this reaction is SN (SN2 or Sy1?). Explanation: Jvcleophile

A: SN2 reactions occur in a single step whereas SN1 reactions are those that occur in 2 steps. SN2…

Q: ropose an efficient synthesis for the following transformation: Br

A: In given reaction bromobenzene is converted into styrene.

Q: ProVide the major prochuct for each following reactuns H more Than one 5 formed, Circk the major…

A: 1) first allylic cation is formed which is electrophile and it attack on Benzene .Ring and product…

Q: abel the Reactants (R), Products (P) and Transition State (TS) ndicate the standard free energy of…

A: Activation energy is defined as minimum amount of  energy  required by the  reacting molecule to get…

Q: Q3/ Draw a stepwise detailed mechanism that illustratés how four organic products are formed in the…

A: The stepwise mechanism to form products are given below- Alkyl halide is 3°. Hence; carbocation is…

Q: soogain aftex gepeatation this single -H š heplacad by -OH

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Q: 6. Explain why halogenation occurs twice in the following reaction. Ch₂ NaOH give both answer asap…

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Q: prounde reagent tocary followngons tormation. out the

A: Answer is explained below.

Q: Draw the product by following the curved arrows. This reaction is an example of a [3,3] sigmatropic…

A: Sigmatropic rearrangement is shifting of sigma bond with the reorganization of pi-bonds in a system.…

Q: What alkene yields each set of oxidative cleavage products?

A: Gentle oxidative cleavage of the alkene in presence of KMnO4, O3 will give carbonyl products. The…

Q: Same reaction as previous question. Which statement(s) is(are) true concerning the rate-limiting…

A: We have to predict the correct statement regarding rate limiting step.

Q: How many transition state/s is/are present in the reaction based from the energy diagram as shown…

A: Given is energy diagram.

Q: Draw the Product(s) and the Step-by-Step Mechanism for the Reactions Shown. Make sure to indicate…

A: the reaction and mechanism are as follows:

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.