CH,CCCH2 Your answer cicc(CH,),CCBR Your answer CH;(CH,),C,H; 6''5

Q: H3180+ H,CH,C- CH,

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Q: H,C-CH-CH, ČH, H,C-CH-CH, ČH2-CH, H,C-CH,-CH2-CH-CH,-CH2-CH3 ČH;-CH, CH2-CH, H3C-CH2-CH2-CH-…

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Q: CH;CH2CH,CH,CH2B1 NH3 G + H + excess

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Q: H3O* но нс H3C---C-C-CH3 CH2CH3 CH,CH3 C-C H3C H H OH

A: The reaction given is Since the O in the reactant is having lone pair electrons. Hence it will take…

Q: Rank the water solubility of the following compounds:

A: Given compounds,

Q: CHy-C=C-H --> CHZCHZ CH3 a) CHS CH3 Oo --> b)

A: here we can make our desired product by first making halides of starting material by reacting one…

Q: OH CH3 II CH2CH3 НО HO- -H- ČO,H ČO2H II IV CH3 CO2H H- -HO- Но -H-

A: Fisher

Q: a. -CH2OH b. -CH2B1 c. –CH(CH3)2 -CH3 OH- -CH,CH,Br H- -CH3 -CI -CH,CH2OH –CH¿OH -CH,CH,CH,Br

A: Priority to the atoms/group of atoms are given according to Cahn-Ingold-Prelog rules/principles.…

Q: N HN, CH2-C-NH2 CH2 O ters. H3N-C-C-N- CH-C-N- O=

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Q: (b) CH3 1. DIBAH CH3CHCH2CH2CO2CH3 2. H30* (d) CO2H CH3OH, ? H2SO4 CH3 он CH;CO,COCH3. Рyпidine (h)

A: Answer  Draw the product of the following reaction

Q: (d) (c) CH3 0 1. LIAIH4 ? 2. H2O H2C-CHCH,CH3 HBr. ? H2C=CHCHCH2COCH3

A: Lithium Aluminium hydride is a strong reducing agent which reduces esters into alcohols. The…

Q: a. H-C-C-H

A: Ozonolysis is a quite important reaction in organic synthesis where unsaturated double bonds undergo…

Q: CH3CH=CHCH,CcOOH ----> CH3COH + HOCCH2COOH

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Q: CH3 CH;CH,C-CHCH; HC/ZnCl2 ÓH CH3 I. CH;CHOH NaOH CH,

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Q: H* H3C-C-0-CH2CH3 H,0 H" 0-H + H,C. H,C HN +

A: The reaction in which and acid reacts with an alcohol to produce an ester is called esterification.…

Q: व) होण्रऔीकर लाय कवnो उमा पईPठठवेपटक वनै झट किनीनजणम् जहकर कीनकह तिलेबनेकमु उेटाइटर्नंदागाউय म्रिोड…

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Q: CH3-CH2-OH Escrna) H Coy 0) 8. CHg-CH2-CH-CHgs EMPJHT

A: Since K2Cr2O7 and KMnO4 are strong oxidising agents. Hence primary alcohols on reaction with them…

Q: 20,²-(aq) + C,H;OH(aq) → CO29) + Cr³+

A: Cr2O72-(aq.)+ C2H5OH(aq.) ----> CO2(g) + Cr3+(aq.)  Step-1: Split into half reaction and balanced…

Q: B. Condense and Name: HH H H H b. H-C-- CH,CH,CHCH,CH,CH, CH,CH,CHCH, a. C. ČH, ČH,CH, HH H H H

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Q: CI Your answer SH H3C, CH3

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Q: (a) Br CH3CHCH₂CH₂CH₂C(CH3)3 (b) -Ō (c) CI CH3 Br

A: According to IUPAC nomenclature we have to first select the parent chain and have to number then .So…

Q: (a) Br2 FeBr, (b) NaCN (c) HO H,SO, 180 °C Major product

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Q: H₂CHN +2 CH3MgBr followed by H + CH3NH₂ B+ NaOH +CH₂I +CH₂OH. H* E +NaNO₂, HC1-F + CH3COCI G -D A с

A: We have to draw the product of following reaction given below:-

Q: CH3 H,CH,C-C-X ČH,

A: Homolytic cleavage leads to the formation of free radicals. Heteroytic cleavage leads to the…

Q: CH3 HgCㅡ-CH=CH-CH: CH -CH3 а. b. H3C- -NH-CH3 O: I

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Q: (CH3)3CCH2CH- CH CH2- Your answer

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Q: g. Н-С-С CH,CH3 h. HICIH

A: A functional group is an atom or a group of atoms that are present in a molecule and is responsible…

Q: Draw curved arrows to show the movement of the electrons as the bond forms.

A: Please find below the curved arrows showing the movement of the electrons as the bond forms.

Q: i some CH =CH2 r ? It CHz Cl

A: The IUPAC name of the given compound is : 5-Chloropent-1-en-3-ol. In this compound third carbon is…

Q: hamess CH3-CH cH3- cH3 -CH cH3-CH cH

A: In IUPAC  nomenclature of ether the most complex group is named as alkane as root word where as the…

Q: What is the configuration of the asymmetric centers in the following compounds?

A: Step 1: Actually, the asymmetric center is the center in a compound where all the groups attached…

Q: Draw a stepwise mechanism for each reaction.

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Q: u OH OH CH₂ CH₂ ‡ Br -CH₂ OH unrelated R He OH strudel isquer H₂Cy Br OH Br CH₂ 3 R

A: R/S system of nomenclature : It is a naming system used for assigning absolute configuration to…

Q: H H3C-C + :CI: H,C - c - ČH3 CH, ..

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Q: H C-ċ-c=c• -C-I エ

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Q: LIAIH, d. CoHs-C-CHз H+ е. CоHs-C-СH NaBH, H+ f. C6H5-C-CH3 Br2 NaOH

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Q: CH,CH, CHg (b) CH, CH,CHg (c) HgC CH3 CH;CH,CHCH,CH,CHCH3 CH;CH-CH;CHCH>ÇCH3 CH3C-CCH,CH;CH3 CH3 HgC…

A: Please find the file attached for explanation

Q: CH3 Brz/H,O A) CH3 CH3 1) BH/THF B) 2) H-О, NaOH CH3 CH3 CH3COOH C) CH3

A: Reaction is called bromination of alkenes. Solvent used is water. In this reaction solvent is very…

Q: -С-NCH-CH3 + HCI H2O H-0 a. ČH,CH3 1. CH3CH2MgBr 2. Нзо* b. CH;CH,ĊCH3 с. + (C,Hs)3P=CHCH3

A: Note: According to our guidelines we are supposed to answer only first three subpart.

Q: н- НО- н- н- CHO -ОН -H -ОН -ОН CH₂OH [H], LiAIH4

A: Here you are asking multiple questions so I am answering one question (Q.7)in this session.

Q: H-CEC-H

A: Organic synthesis is a process of making organic molecules in a convenient pathway.

Q: 1. 2. CH-CI 12- - --> OH XI OCH3

A: " Since you have posted a question with multiple sub-parts, we will solve first three sub-parts for…

Q: g. H;C NH, h. i. H* H;C-C~o-CH2CH3 H,0

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: Identify the catalyst in each equation.

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Q: Br | CH, - CH, - C - CH,-CH - CH, S-H S-H S-H .CI S-H

A: The naming of organic molecules takes place according to IUPAC naming system. The first step…

Q: CI CH,- CH, - CH -CH-СH,-CН, Br

A:

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.