AlCl3 + Cl,

Q: Add curved arrows to show how carbocation A is converted tocarbocation B. Label each new σ bond…

A: Given:

Q: HO,

A:

Q: Step 3: Complete the resonance structure of the enolate form. Omit curved arrows. Erase Select Draw…

A: Keto-enol tautomerization: It is a chemical equilibrium between two structures keto and enol form.…

Q: + i) +CH3-MgX H30

A: Grignard reagent :- Alkyl magn esium halide (RMgX)  is called grignard reagent. It is highly polar…

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

A:

Q: Fill in the blanks: Polar mechanism because it stabilizes the solvent favors the SN1

A: SN1 reaction is commonly known as unimolecular nucleophilic substitution reaction ,  rate of…

Q: Select the member of each pair that shows the greater rate of SN2 reaction with KI in acetone.

A:

Q: at changes in color take place when KMnO4 reacts with an alkene

A: To tell the change in color when KMnO4 reacts with an alkene.

Q: Consider the following reaction. cat. ACOH el H2N-NH2 Toluene (reflux, remove H2O) a. Draw a…

A:

Q: Supply synthetic routes to the following molecules using the indicated starting materials

A: The synthetic route for preparation of 2-hexanol is as follows,

Q: ОН ТВHS + NaOCl EtOAc/H,O + NaCl + H½O

A:

Q: Draw all constitutional isomers formed in attached elimination reaction.Label the mechanism as E2 or…

A: The base and the type of alkyl halide in a given reaction determine the mechanism. In the given…

Q: Give the curved arrow mechanism for the transformation below CI H2N-NH2 NH pyridine NH

A: The answer is given as follows

Q: (üi) from NH2 CH3

A: 3) The mechanism of formation of isoquinoline  has been outlined below

Q: BH3•THF HO.

A: Detail mechanistic pathway is given below

Q: Select the member of each pair that shows the greater rate of SN2 reaction with KI in acetone.

A: The addition of nucleophile and removal leaving group takes place in simultaneously in SN2 reaction…

Q: 3. Rank the following in order by the rate in which they could participate in an SN1 reaction (“1"…

A:

Q: H;0"/H;O/A HO.

A:

Q: O, N. Na OHCag) + Nacl

A: Acid-Base reaction:  In chemistry acid-base reaction is the fastest reaction and salt will be formed…

Q: Complete the Diels alder reaction. Show the mechanism with curved arrow s .CN

A:

Q: Draw all constitutional isomers formed in attached elimination reaction.Label the mechanism as E2 or…

A: The base and the type of alkyl halide in a given reaction determine the mechanism. In the given…

Q: 1: NaOH 2: D;SO4 S-Methyl 3-methylbutanethioate

A: The reaction of carbonyl compounds with NaOH results in (SR) nucleophilic substitution reaction.…

Q: Select the member of each pair that undergoes SN1 solvolysis in aqueous ethanol more rapidly

A: In SN1, the rate determining step is formation of carbocation and order of the substrate that…

Q: с. ano H+ HO, HO

A:

Q: AICI

A:

Q: HO3S- -CH3 Br CH3

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

Q: Mechanisms. Give the curved-arrow mechanism for each reaction indicated below. Use and attach extra…

A: Hu

Q: nechanism for the following transformati Br2 + HBr Br CH2OH

A: The given organic reaction is the reaction between alkene and bromine followed by ethanol,  results…

Q: 1. Draw the curved arrow mechanism for the given reaction and write the product. CF₂CO₂H

A:

Q: What type of carbocation is shown? (+)

A:

Q: NH2 CH3 OH Br CH3MG Br

A: Reaction 1: CH3OH acts as a base and abstracts the acidic proton from the amine. This PhNH- moiety…

Q: Please draw the arrow pushing mechanism for the following ellmination reaction to glve the Hofmann…

A:

Q: Select the member of each pair that shows the greater rate of SN2 reaction with KI in acetone.

A: SN2 reaction is as type of reaction mechanism in which attacking of nucleophile and…

Q: Use the Hammond postulate to explain why (CH3)2C = CH2 reacts faster than CH3CH = CH2 in…

A: The addition of HX to the alkene is the type of the electrophilic addition reaction. In this…

Q: Select the member of each pair that shows the greater rate of SN2 reaction with KN3 in acetone.

A: SN2 reaction rate depends upon the steric effect. Higher the steric hindrance, lower would be the…

Q: Draw a complete arrow pushing mechanism that explains the following: Br NBS hv Br

A: N-bromosuccinimide (NBS) is used as allylic brominating reagent. 3,3-dimethylcyclohexene on…

Q: Select to Draw OsO4 (catalytic) NMO OH OH

A: Write reactant of the given product---

Q: Draw the following compound on your separate sheet. (1S,2S)-5-(2methylepoxy)cyclopent-2-enol

A: Given name, (1S,2S)- 5- (2 methylepoxy)cyclopent-2-enol

Q: Explai all steps to Determine the Directing Effects of a Particular Substituent ?

A: The characteristic reaction shown by benzene and other associated compounds is electrophilic…

Q: SN2 mechanism

A: no, polar solvent dissolve the substrate and nucleophile but do not participate in hydrogen bonding…

Q: CH3-C=CH А B Hg2*, H*

A: Terminal alkynes on reaction with sodium amide(NaNH2) produces corresponding acetylide which attacks…

Q: НО. ОН

A: Addition of hydrogen to a molecule or removal of oxygen is called reduction. Removal of hydrogen to…

Q: 3. Rank the following in order by the rate in which they could participate in an SN1 reaction ("1"…

A: An SN1 reaction is proceed by the formation of a carbocation (an ion that contains a positive charge…

Q: (a) Explain with suggestive mechanism why BuLi undergoes 1,2-addition with a, B- unsaturated…

A:

Q: Draw the mechanism for the reaction of cyclohexene with HCl.

A: The cyclohexene reacts with HCl via electrophilic addition.

Q: H-CI

A: Protonation of alkene give more stable carbocation. Addition of chloride ion to carbocation gives…

Q: What type of carbocation is shown?

A: As we can clearly see that the positive charge (cation) containing carbon is attached to two carbon…

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.