1) HNO3 / H2SO4 Br 2) Zn / HCI CH3CI / AICI3 O=

Q: most taci cofommer below CH3 CH3 OCHS OCHS OC,Hs CH3 OCHS CH3 CH3 OCHS OCHS CH, OCeHs H3C- CH3 CH3…

A: In the given cyclohexane derivative, the presence of substituents and their size decides the…

Q: b. C. O d. e. H f. HO -ОН -OH Na₂Cr₂O7 H₂SO4, H₂O -OH OH xs CrO3 H3O+ acetone 1) DMSO, (COCI)2, ? 2)…

A: we have to draw the major product for the given reactions

Q: Br 16. CH3CHCH2CH2ČOH H H 17. HO2C" "CO2H CH3 CN 18. CH3CHCH2CHCH3

A: Write IUPAC name of the given structures--

Q: What compounds are obtained from the following hydrolysis reactions?

A: Since you have posted question with multiple sub-parts, we are entitled to answer the first 3 only…

Q: e). CH,CH2CHCH3 ci CH3 i). CH3-C-CI a). CH3CH2CHCH3 CI ci CH3 CH2CI b). CH3-C-CH3 f). CH3CH2CH2CH2CI…

A: * Two or more compounds having same molecular formulas but different structures i.e IUPAC names are…

Q: CH3 HCI CH3 CH3 CH3-CH-OH ZnCl2 CH3-CH-CI CH3-C=0 BCD DCB

A:

Q: CH2-CH3 CH3 -C- chz CH3 H -CH3 CH3 Pel4 ce CHS Heas PBY3 BY L 7 CH3 1Naon

A: Rules of IUPAC nomenclature First, we have to find the longest carbon chain that is continuous.…

Q: What is the major Hofmann elimination product formed from each amine?

A: a. The quaternary amine for the given amine is,

Q: a) b) CH3-CH₂- c) d) e) f) 0 O-CH₂-CH2-CH3 de CH3-CH-CH-CH3 CH3 OH -od x OH

A: The given problem is based o nomenclature of organic compounds.

Q: CI SN2 + HO CH;OH or CI SN2 + НО II CH3-S-CH3

A:

Q: (a) excess NH3 + Ph-CH₂ CH₂ CH₂ Br (b) 1-bromopentane (1) NaN3 (2) LiAlH4 (3) H3O+

A:

Q: CI CI он OH HO А — Clz/H20 В -СНCI3/КОН С — 1. Оз/СH2CI2 2. Zn/HзО* D- HIO4/THF/H2O E - H3O*/THF…

A: A. Cl2/H2O: This causes conversion of alkene to trans halohydrin B. CHCl3/KOH: This generates…

Q: CH3-CuLi а) HNO b) он

A: The question is based on the concept of organic reaction mechanism. we have to write the product…

Q: Rank the following Newman projections in order of increasing energy.

A: Conformers can be defined as the structures of same molecule which are formed because of the…

Q: What is the major product of each of the following reactions?

A: Since you have posted multiple sub-parts, we are entitled to ans only the first three.

Q: CH3 CH3 CH C-C=CH CH3-CH,CC=CCH, CH3 IRE REI H3C H3CH2CC=CCH2CH3 H,C HCC CCH,CH3 ERI RIE Select one:…

A: Ozonolysis mechanism:

Q: CH3 AICI3 + CH2-CH-CH2-CI CH3 CH3 CH2-CH-CH3 .ĊH-CH2-CH3 (а) (b) CH3 CH3 -CH3 CH2-CH2-CH2…

A:

Q: CH3 CH3-CH2-CH-CH3 (b) (с) (а) H3C CH3 CH3 CH3 H3C- CH3 Но CH -CH- -CH3 (f) (d) CH3 CH3

A:

Q: d. HO CH₂CH-C3 NH₂ I 01 N-CHCH₂ OCH 3

A:

Q: ÇI CI -CH3 +2Zn 2ZnCl2 + Č CI Cao +NazCO3 + CH;CHCOONA + NaOH CH3 d.e. 2 CH3CHBR + 2Na 2NaBr + CH3

A: Given,

Q: (a) CH3 CH3 (b) ÇO2H (c) Br CHCH2CH2CHCH3 H3C CH3 Br (d) Br (e) F (f) NH2 CH2CH2CH3 NO2 NO2

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

Q: Which of the following reactions lead to the formation of an amide?

A: In reaction A, the carboxylic acid has no good leaving group. So, the reaction cannot occur. In…

Q: CH3 CH3CH₂CH=CH-C-CH₂-CH3 CH3 H₂C-CH₂ TIT HC=CH L F

A: Given compounds are :  Give the IUPAC names of the given compounds :  The suffix use for alkene…

Q: OH + H₂CRO4 → (a) 1. 2. H₂C=CHCH3 + H*/H₂O → (b) 3. CH3CH₂CH₂Br + LiAlH4 → (c)

A:

Q: 5. (X)C,H¬OC1- NH3 →C¢H„ON- Br2 →CH3CH2CH2NH2; Compound (X) i : КОН CH3 (b) CH3 (a) (c) -HO- (d) cl-…

A: To solve this problem we have to complete the given chemical reaction .

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: Issily (CH3-CO)20 а. b. CH3 (CICH2-CO)20 (CH3-CH2-CH2-CH2-CH2-CO)20 C. d. е.

A:

Q: А.) CH2=CHCH2COCHCH(CH3)2 CH3 CH2 В.) CH3CH(CH2)3COCI C.) C.) CoHsCH2OCO(CH2)7CH3

A:

Q: Vhich of the following is not a constitutional isomer of CH3CH2COOH? OA) CH3CH2COOCH3 OB) CH3COOCH3…

A: The compound given is CH3CH2COOH.

Q: CH3 CH3 H3C- CH3 A) I CH, CH, CH „CH3 B)II C) II CH, IV CH, D) IV CH3 CH3

A: In the given chair structure , all of the groups are on the same side ( i.e above the plane )

Q: a) b) c) d) Br H ce CHz CNFCH-CH3

A:

Q: H. CH3 H. CH2CH3 H CH3 H. CH,CH3 H. H. CH3 H CH2CH3 H CH3 CH3

A: Projection 1 is the correct answer because when we see from C2 and C3 axis then it will form and…

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: NH₂ 1) Acetone/ -H₂0 2) CH₂(CO₂Et), NaOCH; O A B. C. D EtO₂C N C) -CO₂Et -CO₂Et B) CO₂Et CO₂Et CO₂EI…

A: In this question, we will draw the structure of the major product after reaction between reactant…

Q: (d) (e) (f) H-CEO- CH3CH₂MgBr H₂O, H₂SO4 HgSO4 1.03 2. H+, Zn

A:

Q: OEC Fe OC CO OC OEC (ii) CH3 (iv) CH3 H3C. CH3 CH3 As (OC):Os- OEU-

A: A complex is a substance wherein a metal ion or particle is related with a gathering of impartial…

Q: 1. Sia BH H3C-C C-H 2. H2O2, OH O A. CH3C(OH)=CH2 O B. (CH3)2C=0 OC. CH3CH2CHO D. CH3CH=CHOH (cis)…

A: This is an example of hydroboration oxidation. This is equivalent to the anti-Markonikoff's addition…

Q: 1. D. A. - CH3 2. OCH, D. C. B. A. 3. Endo Praduct: A. В.

A:

Q: OCH2CH2CH3 a) CH;CH(OH)CHCH(OH)CH(CH:)CH3 H;C. но Br b) e) (CH3):CHCH2OCH;CH3 но. -CH3 CH3 c) bllege…

A: 1. We have to give the IUPAC names of the following given compounds as follows in step 2:

Q: ŅH2 + H2SO4 NH2 CH3 CH3CH2B., AICI3 NH2 „CH3 CH3CH2BR + NH2 „CH3 H3C-C CI + O=

A: (1) When 2- methyl aniline treated with Sulfuric acid, it gives para amino benzene sulfonic acid.…

Q: H2SO4 CH;CHCH2OH CH3 H2SO4 2 CH,CHCHCH,CH3 CH3 Majo CHaCH-CHCH3 +2KOH Br Br

A: ->H2SO4 is a dehydrating agent which form alkene. ->Alco KOH is used for elimination reaction.…

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

A:

Q: 1) NaBH4 2) CH,CH,ОH OCH2CH3 (А) (В) CH2OH OCH,CH3 ОН (С) ОН (D) .CH2OH OCH2CH3

A:

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: (c) CH2CHCOCHCH3 ja) CH3 (b) CH3CHCH,CH,ČCI CH2ÖNH2 CH3 CH3 (e) OCHCH3 ČH3

A: All chemical compounds can be named with certain rules which are purposed by IUPAC. It purposed to…

Q: c) d) e) f) H.C -CH3 -CH3 NaCN ОН 1) BrMg CH OH H₂SO4 CH3 2) HạO* H OCH OCH _NH2OCH3 CH3 CN CH 3 -он…

A:

Q: CH3 CH3 CH3 NaOCH3 H CH,0CH CH3 CH;0 CH2CH3 CH2CH3 Br SN2 H VWX XWV O VWX O XwV

A: The SN2 reaction is a nucleophilic substitution reaction. It is a one-step reaction where the…

Q: CH3 HCI CH3 CH3 CH3-CH-OH ZnCl, CH3-CH-CI CH3-C=0 BCD DCB BCD DCB

A: Lucas reagent: The mixture of HCl and ZnCl2 is a Lucas reagent which is used for the test of…

Q: H3C CH3 a. N. b. CH3 c. CH3-CH-CH2-Ċ-OH с. d. CH3-CH2-CHBR-CH2-CHO CH3-C-NH–CH3 е.

A: During the IUPAC naming of a chemical compound, we have to remember the following main points --- i)…

Q: А. B. C. D. HO w.. H3C CH3 CH₂ H CH3 CH3 CH3 CH3 HC3 CH3 HC3 CH3 Ž HC3 CH3 OH OH om CH3

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.