Draw the structure of the product of following transformation. [1] (CH₂=CH)₂CuLi [2] H₂O workup

Q: v Correct Part B Spell out the full name of the compound. (z)-2-hexene Submit Previous Answers…

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Q: Which hydrogenation would convert but-2-yne to (Z)-but-2-ene? A) Na/NH3 B) H₂, Pt C) Lindlar's…

A: Here we to predict the reducing agent in which can convert but-2- yne  into (Z)- but-2-ene and (E)-…

Q: Draw a structural formula for the major product of the reaction shown. H3C Cl2 H3C H20 • Show…

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Q: Label each substituent as an ortho, Para, or meta director. COOCH3 NHCOCH3 CH3

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

A: The given reactant is a triester. It reacts with sodium hydroxide (NaOH) resulting in the formation…

Q: CH2-0-C-(CH2)4CH=CHCH,CH=CH(CH2); CH3 3 H2 CH-O-C-(CH2)4CH=CH(CH2)2CH3 Pt ČH2-0-C-(CH2)4CH3

A: Hydrogenation of lipids

Q: Draw the products formed when (CH3)2C=CH2 is treated with following reagent. [1] BH3; [2] H2O2, HO−

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Q: Draw the major organic product for the reaction: Br NaCI H20

A: Given,

Q: Draw the alkene that would react with the reagent given to account for the product formed. ? + HCI…

A: Detail

Q: Draw the two major products obtained in the reaction shown. CH2C12 Br2 (one equivalent)

A: 1,2-Addition involves the formation of a single product where the added group is attached to the…

Q: `CF3 NaH DMSO

A: DMSO is a polar aprotic solvent which favour E2 elimination.

Q: н ОН н н Ян

A: Functional groups   Functional groups are some special atoms which gives identity to the compound.…

Q: 1) 2) 03 H₂O

A: These reactions are also important in advanced oxidation processes. Molecular ozone acts as a…

Q: Br "cEN,

A: Cyanide ion is a weak base and a strong nucleophile. So, It will react with 2-bromocyclohexanone via…

Q: CH3(CH2)4Br

A: The name will be hept-1-ene

Q: Draw the major organic substitution product for the following reaction: GI CH3CH2OH isopropyl…

A: The major organic subtitution product for the following reaction is:

Q: 8) 1,1-dimethyl-3-cyclohexene h) 2-ethyl-4-pentene i) 3,4-dimethyl-2,4-cyclopentadiene

A: Note : as per our company guidelines we are supposed to answer only first 3 sub-parts. Kindly repost…

Q: Name this compound according to the IUPAC system, including stereochemistry. Br CH 2,6-dibromo

A: Name the given organic compound include stereochemistry---

Q: 1. Which alkene is the major product of this dehydration?

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Q: Name your compound according to the IUPAC system. Include stereochemistry (E/Z/R/S). H₂C H₂C

A: For IUPAC naming following steps are required->First of all select the largest carbon chain…

Q: Draw a reasonable arrow - pushing mechanism that explains formation of the given products. HBr, A O…

A: Given a reaction to heat and to draw its mechanism.Here a highly stable Benzylic carbcation forms…

Q: (CH3CH2)2NH + H2SO3

A: Here CH3CH22NH will act a Lewis base and abstract the proton from H2SO3.

Q: 9) Draw the conformer structure, Newman projection, before elimination and the elimination product…

A: Due to strong base and 3° C it gives E2 elemination reaction

Q: What is the IUPAC name of this compound? CH3CH2 C CH(CH3)CH2CH(CH3)2 H H

A: IUPAC naming for hydrocarbons includes the following steps:Identifying the longest continuous carbon…

Q: TReview TOpics] [References Draw a structural formula for the major product of the reaction shown.…

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Q: What is the major product of the following reaction? (CH,),CO Br (CH3) COH " IV

A: Reaction OverviewThe reactant is tert-butyl bromide (CH3)3CBr(CH_3)_3CBr(CH3​)3​CBr.The base used is…

Reactive Intermediates

In chemistry, reactive intermediates are termed as short-lived, highly reactive atoms with high energy. They rapidly transform into stable particles during a chemical reaction. In specific cases, by means of matrix isolation and at low-temperature reactive intermediates can be isolated.

Hydride Shift

A hydride shift is a rearrangement of a hydrogen atom in a carbocation that occurs to make the molecule more stable. In organic chemistry, rearrangement of the carbocation is very easily seen. This rearrangement can be because of the movement of a carbocation to attain stability in the compound. Such structural reorganization movement is called a shift within molecules. After the shifting of carbocation over the different carbon then they form structural isomers of the previous existing molecule.

Vinylic Carbocation

A carbocation where the positive charge is on the alkene carbon is known as the vinyl carbocation or vinyl cation. The empirical formula for vinyl cation is C2H3+. In the vinyl carbocation, the positive charge is on the carbon atom with the double bond therefore it is sp hybridized. It is known to be a part of various reactions, for example, electrophilic addition of alkynes and solvolysis as well. It plays the role of a reactive intermediate in these reactions.

Cycloheptatrienyl Cation

It is an aromatic carbocation having a general formula, [C7 H7]+. It is also known as the aromatic tropylium ion. Its name is derived from the molecule tropine, which is a seven membered carbon atom ring. Cycloheptatriene or tropylidene was first synthesized from tropine.

Stability of Vinyl Carbocation

Carbocations are positively charged carbon atoms.  It is also known as a carbonium ion.