Provide a mechanism for the following transformation. кон, д

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: Propose an efficient synthesis for the following transformation: ОН

A: In the above synthesis But-1-ene is converted to pentan-3-ol.  The above reaction proceed through…

Q: Tamoxifen is an estrogen receptor modulator that is used in the treatment of breast cancer. Provide…

A: In organic synthesis, suitable reagent converts the reactants into products. Reagents attacks with…

Q: Propose a reaction mechanism for the following transformation:

A: Answer is explained below.

Q: Provide the necessary reagents for the following transformation. Ph `Me Ph `Et

A: 1,3-diketone contain a acidic hydrogen and this hydrogen can be removed in the presence of base to…

Q: Provide a mechanism for the following transformation: OH Cro3 но. H30*

A: The mechanism of the given reaction is given below,

Q: Meo Meo Me 5. Me Meo

A:

Q: Provide a detailed arrow-pushing mechanism for the following transformation: Me PHOH PhO. Et Мe Me…

A:

Q: 14. Propose a mechanism for following transformation. M₂O 0

A: In this question, we will write the details mechanism steps by using curved arrows for the given…

Q: Provide the missing reagents required for the following transformation: OH OH

A: Alkene reacts with peracid, RCO3H (such as metachloroperbenzoic acid, mCPBA) to form an epoxide. The…

Q: Decytospolides A and Bare fungal natural products that are toxic to some cancer cells, In a…

A: Concept : 1) NaH is used as base for deprotonation.  2) Grignard reagent is used as nucleophile here…

Q: Propose a mechanism for the following reaction:

A: The given reaction is represented as follows:

Q: 4) Provide a list of reversible vs irreversible carbonyl additions.

A: A question about reversible and irreversible carbonyl addition reactions, which is to be…

Q: 4. Provide a arrow pushing mechanism for the following transformation. H3O+ Br2

A:

Q: Propose a mechanism for the following reaction:

A:

Q: Identify R and S in the following reaction sequence, and draw a mechanism for the conversion of R to…

A:

Q: 5. Propose a plausible arrow pushing mechanism for the following transformation. он H+

A:

Q: Propose a synthesis for the following transformation.

A:

Q: Propose a mechanism for the following reaction. CI -NH2 -NH-

A:

Q: Propose an efficient synthesis for the following transformation:

A:

Q: Give the structure of compounds A to E in the following reaction sequence.

A:

Q: 3. (A) Provide the necessary reagents to accomplish the following transformation. CH2BR CH2OH CH2CH3…

A:

Q: Propose a mechanism for the following reaction and develop it.

A: Given Reaction is known as Dienone phenol rearrangement reaction .

Q: Propose a plausible synthesis for the following transformation:

A: Here we have to propose a plau synthesis for following transformation

Q: O₂N. Br

A:

Q: PROPOSE A POSSIBLE SYNTHESIS FOR THE GIVEN TRANSFORMATION

A:

Q: Propose an efficient synthesis of each of the following transformations:

A:

Q: Mustard gas, Cl¬CH2CH2¬S¬CH2CH2¬Cl, was used as a poisonous chemical agentin World War I. Mustard…

A: Sulfur in mustard gas is more nucleophilic than other corresponding oxygen compounds. This is due to…

Q: Propose a mechanism for the following transformation: CI HCI H20 +

A: Alcohol reacts with an alkyl halide to form an alkyl chloride. The reaction proceeds with an SN1…

Q: a Propose an efficient synthesis for this transformation.

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

Q: Provide a mechanism for the following cyclization to make a spiroketal: H,SO4, H,O НО OH spiroketal

A: The reaction taking place is given as,

Q: (e)

A: The given synthesis is of (2-methylprop-1-en-1-yl)benzene from toluene. The reaction follows a…

Q: c) d)

A:

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

A: Alkenes are species which readily reacts with electrophile.

Q: Propose a synthesis for the following transformation: HO

A:

Q: Provide the mechanism for the following transformation: NaCN CN + Naci

A:

Q: CH3 CH=CH, H*

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

Q: S Na* SCH CH3 a thioester ethyl thiolate

A: It is a general case of attack of RS- nucleophile on Electron deficient Carbonyl Carbon to form…

Q: `OH ZI

A:

Q: Propose an efficient synthesis for each of the following transformations: .CI

A:

Q: Propose a mechanism for the following reaction:

A: Please find below the reaction mechanism

Q: Propose an efficient synthetic route for the following transformations:

A: We can prepare this molecule by Michael addition reaction.

Q: HCI + H20

A:

Q: Propose a mechanism for the following transformation CI HCI H2O +

A: Alcohol reacts with an alkyl halide to form an alkyl chloride. The reaction proceeds with an SN1…

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: Propose a plausible mechanism for each of the following transformations.

A: A detailed mechanism explained for first three reactions are given below

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: но CH3

A: Applying concept of organic synthesis and reagent.

Q: 4. Propose an efficient synthesis for each of the following transformations. (d) (e)

A: Interpretation -  To propose an efficient synthesis root for each of the following given…

Diol

In chemistry there are so many chemical compounds that have a hydroxyl group but a chemical compound having two hydroxyl groups (-OH) is termed as a diol. It also implies the presence of two alcohols whereas polyols contain two or more than two hydroxyl groups (-OH). Glycol or 1,2-diol is an aliphatic diol that has two alcohol groups on adjacent carbon atoms. In industries, the most commonly used diol is ethylene glycol.