Propose a stepwise mechanism that accounts for the transformations below.

Q: Make a proposal for an efficient synthesis for the transformations listed below: HO,

A:

Q: Propose an efficient synthesis for the following transformations

A: synthesis of following transformations

Q: Propose a synthetic path to perform the following transformations

A: Answer - Synthetic  path  to perform the following transformation -

Q: From the table of available reagents select the one(s) you would use to accomplish the…

A: For the transformation of two reactions following reagents are required

Q: Starting with 3,3-dimethylbut-1-ene and prop-2-inonitrile, propose a synthetic route for the…

A: Both retrosynthesis and forward synthesis are shown with details mechanism in image.  At first…

Q: Propose a synthesis of the following molecule using a Robinson Annulation. Each starting material…

A: 1 First  findout  starting  material:-     we  will  used  Retrosynthesis Analysis  for product…

Q: a. 10-0 b. -

A: Detail mechanistic pathway is given below to carry out the following conversion

Q: Propose a reaction mechanism for the following transformation:

A: Answer is explained below.

Q: Suggest a mechanism on how to achieve the final product (including reagents). Ty! NME2 Ph Ph CI

A:

Q: Propose a synthetic pathway to generate the molecule below. You may use benzene, alcohol, and alkyl…

A: This molecule can be generated by several step using malonaldehyde as a starting material.  There…

Q: Propose an efficient synthesis for the transformation below. Enter the appropriate code from the…

A:

Q: Propose a plausible synthetic route for the following conversions. Show all reagents and…

A: The hydrogen attached to the alkynes are acidic becasue it is attached to sp hybridised carbon. So,…

Q: Show how you would accomplish the following synthetic conversions efficiently and in good yield. You…

A:

Q: 5. Propose a plausible mechanism for the following transformation:

A: Given that : We have to propose a mechanism for the following transformation :

Q: Propose an efficient synthesis for the transformation below. Step 1 .Step 2

A: In this question, we want to identify all two step Reagent ( step-1 and step-1 ) for this given…

Q: Propose reagents needed to achieve the following transformation. CI, CI

A: it is an elimination reaction, here we need strong base to convert this reactant into alkyne. 2 mol…

Q: 1. Complete the following transformation and provide the detailed steps (a) NH2 OH

A: In the given transformation the alcohol is converted into an amine with an extra carbon atom. The…

Q: Propose a synthesis for the following transformation from benzene using any inorganic and carbon…

A: Given condition:  2 carbons of reagents and lesser carbons and the starting material is the benzene;

Q: 10. Provide a mechanism for the following transformation using curved arrow notation. What is unique…

A:

Q: D phmgBr, Etz0. locts OCH3 2) Hz0

A: Given,

Q: Propose a mechanism for the following reaction:

A: The path followed by the reactant to result in the formation of products is known as mechanism of…

Q: Show all steps necessary to accomplish the following conversion (after each reagent provided show…

A:

Q: OH CH3 OH CH3 CH3 CH3 OH CH3 OCH3

A: Organic reaction mechanisms.

Q: 3) write a detailed mechanism for the following reaction: Br hv light + HBr + Br2

A:

Q: Addition of one equivalent of ammonia to 1-bromoheptane gives a mixture of heptan-1-amine,some…

A: a). The addition of one equivalent of ammonia to 1-bromoheptane up to the formation dialkylamine is…

Q: Propose a synthetic route for the following transformation: ?

A: Alkenes are species which readily reacts with electrophile.

Q: Propose an efficient synthesis for the following transformation, provide all necessary reagent(s)…

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: Propose a synthetic route (using all reagents and materials necessary to perform the following…

A: SOLUTION: Step 1: 3-methyl -2-butanol on dehydration in the presence of strong acid like sulphuric…

Q: Provide a stepwise synthesis that will accomplish the following transformation. Show reagents, but…

A: The stepwise synthesis given as accomplish the following transformation

Q: Suggest a) OH Br OH b) с) O-CH3 HO

A:

Q: CH3 CH=CH, H*

A: The given reaction, When 2 molecules of styrene is treated with aqueous sulfuric acid,…

Q: Br

A: Below attached file showing the details answer.  All the best.

Q: Advanced Electron Pushing!! Provide a detailed, stepwise mechanism for the following…

A: NaOMe is very strong base so it take acidic hydrogen nearest to the carbonyl group.

Q: Propose an efficient synthesis for the transformation shown below. Provide explanations for each…

A:

Q: b) Provide the synthons and synthetic equivalents for the following compounds. i) Synthons:…

A:

Q: 1. Show a detailed mechanism for the following reaction and give the structure of the major product.…

A:

Q: 1. Propose two syntheses of the following compound, each using a different Gilman reagent.

A: Gilman Reagent is the Lithium dialkylcuprate. It is used for the formation of C-C bond.

Q: directions if you wish.) 3. Provide a complete curved-arrow mechanism for the following…

A: In Gabriel synthesis, potassium phthalimide gives a nucleophilic substitution reaction with a…

Q: Show and explain reagents and expiramental conditions to synthesize each compound from 1- propanol.

A: (a) 1-propanol transforms to prop-1-ene in presence of acid and heat. (b) Prop-1-ene transforms to…

Q: Which reagent would best accomplish the following transformation?

A: CH3CH2CH2CH2OH ---------------> CH3 CH2CH2CHO The best reagent used to oxidize 1-Butanol to…

Q: I. Propose a one-step synthetic route to get the following compound using only SN2. Explain. H3C=…

A:

Q: HCI + H20

A:

Q: Choose the best reagent (A-E) for carrying out the following conversion from the list provided…

A: Given : structure of reactant and products.  Here oxidation of alcohol is happening.

Q: Propose a synthesis of the following transformation. Number your steps with the names of each…

A: When alkane treated with halide (Chlorine or Bromine) in presence of sunlight or heat then Alkyl…

Q: 3.

A:

Q: NH2 Zエ

A: Here is the conversation of 1° amine to 2° amine.

Q: Provide reagents needed to bring about the following transformation.

A: Reagent is a substance which is more reactive in nature and it attacks on the less reactive…

Q: x

A: Ozonolysis Treatment of an alkene with ozone followed by a suitable reducing agent to break down…

Q: Propose a sequence of steps to perform the following transformation

A: Given,

Q: HO `MgBr OEt

A:

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.