6. a) Propose a reasonable mechanism. OMs H,0 heat

Q: Tell the product from the reaction. And tell (SN2 , SN1 , E1 , E2)

A: The reaction of secondary and tertiary alkyl halide with tertiary butoxide is mostly elimination…

Q: 2) Show an acceptable mechanism for the following transformation using proper curved arrows. HO

A:

Q: Write the complete stepwise mechanism of the following reaction. Show all electron flow with arrows…

A:

Q: 2. Provide all the suitable reagents required to convert each reactant to the product given. Draw…

A: (a)

Q: Predict the mechanism of the rection below.

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: 3. Draw a detailed arrow pushing mechanism for the following reaction H i. Og, ii. PPH3 CH2CI2 H

A:

Q: 1. LDA (slight excess) 2. CH3CH2I

A: LDA is a sterically hindered strong base. LDA is the best reagent to synthesize the kinetic enolate.…

Q: (c) OH H* ?

A:

Q: 6. Determine whether each reaction occurs by an Sn2, Sn1, E1, and/or E2 reaction. Provide a detailed…

A: Hello. There are multiple subparts to this question. The first three subparts have been solved. To…

Q: A B гон NO2 но D

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: H,O, H,SO,(cat)

A: Hydration of alkynes gives ketone. If the alkyne is terminal, markovnikov's rule follow. If the…

Q: Which mechanism is going to predominate under these conditions? A SN1 B SN2 LHOT HCI or C E1 D E2 O…

A:

Q: Bonus: Propose a mechanism Must be perfect for any points NaOEt OEt EtO EtO HOE!

A: Given reaction,

Q: 4. Propose a mechanism, using curved arrow notation, to account for the formation of the following…

A: In the given reaction the alkyl iodide reacts with ethanol to give a substitution and elimination…

Q: 7.4 Propose a detailed mechanism for the reaction below, s

A:

Q: 4) Draw all mechanistic steps (initiation, propagation, termination) for the following…

A:

Q: What

A: A) potassium tertbutoxide is stearicall hindered reagent so Hoffman product is major.

Q: 3) write a detailed mechanism of: OH он CHIČCI AICL3

A: The above reaction is an example of friedal-craft acylation reaction . It is a type of electrophilic…

Q: HCI H20 +

A:

Q: 4. Provide the reagent(s) needed to complete the following reaction scheme. Provide the complete…

A:

Q: How is this incorrect and what is the correct mechanism?

A: Given : We have to tell what will be the correct mechanism.

Q: 2) Propose a mechanism for the following reaction (show all arrow pushing). Note that DgO* has…

A: Two molecules which have same molecular formula but different connectivity and they are easily…

Q: HN CH3B H,0 H* (cat)

A:

Q: (a) PHOOC-CH,-C-CH,-COOP. (1) KCN, A (2) H,0® (o) СООН Onl

A:

Q: 2) Provide a detailed mechanism for the addition reaction shown below. State the regiochemistry and…

A: Given : structure of reactant and product.  This is a electrophilic addition reaction.

Q: III. Give a detailed mechanism for the following reaction: HO, CI

A: Given reaction: We have to write the mechanism of the reaction.

Q: CH3 + НаС — сн н

A: We have to predict the mechanism for formation of given product via Michael addition.

Q: 2. Predict the product and show mechanism.

A: When a carbonyl compound reacts with a primary amine, we get an imine.

Q: Provide a reasonable mechanism that provides the major product for the reaction scheme provided…

A: The reaction given is,

Q: a) ОН ОН b) CI HO

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

Q: 10. For each set of reactions, 1) identify the reaction mechanism as SN1, Sn2, E1, and/or E2 (write…

A:

Q: HO: What is wrong with the mechanism described below?

A:

Q: Show how a 1,2-shift forms a more stable carbocation from each intermediate.

A: The shift occurs in ionic species .and the shift males the carbocation more stable.  In 1st…

Q: 10. For each set of reactions, 1) identify the reaction mechanism as SN1, SN2, E1, and/or E2 (write…

A:

Q: "ropose a mechanism for the following reaction. но H,SO, + H,0

A:

Q: Complete the reactions given below, write down the type of mechanism (SN1, SN2, E1, E2

A: SN1 and SN2 reaction require weak nucleophile and strong nucleophile.

Q: down the product

A: Given:

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

A:

Q: the major and minor products from the following reaction: (Draw the structure of all reactants and…

A:

Q: What is the best way to remeber the differences between Sn1, Sn2, E1 and E2 reations?

A: The best way to remember differences between SN1,  SN2, E1 and E2 reaction is that

Q: Write the correct mechanism and major product for a), and indicate the reagent needed for b) to…

A: Two question based on alkenes, which are to be accomplished.

Q: Write o o mechanism to hronsform Compound A to B NH2

A: For reaction 1, we will use aniline (which is used as polymer)  For reaction 2 and 3, we will use…

Q: From each pair, select the stronger nucleophile. Q.) CH3SH or CH3S-

A: The species which make a covalent bond by donating a pair of electrons is termed as nucleophile.…

Q: 3. Provide the complete mechanism for each of the following reaction. Н-Br

A: Provide the complete mechanism for each of the following reaction.

Q: HO OH H+ to

A:

Q: H.SO Pseudionene B-inone

A:

Q: explain why a polar aprotic solvent speeds the rate of an SN2 mechanism

A: A polar aprotic solvent is a solvent that lacks an acidic proton and is polar.  Polar aprotic…

Q: Show complete mechanism including transition state for an SN, reaction of a specific chiral alkyl…

A: Hi! Since there are multiple questions posted. We are answering first question. If you need further…

Q: Give the mechanism given bleow reactions with curved arrow and all format harges ? 1-ct y

A:

Q: Find the diene and dienophile for the following product (retrosynthesis): ? + ? B B

A: Retrosynthesis: When Reaction  is carried out from product to Reactant side Then reaction is called…

Alkynes

Alkynes are organic compounds that contain at least one triple bond between carbon-carbon atoms. They are a series of unsaturated compounds with a general molecular formula, CnH2n-2.