Br d. f. CI Br a. c. e. b. н— сн, CH2CI Н НС—0 НО Н- -ОН CH3 CI- CH3CH2 -Br Н CH Н н CH3 н Br НО CH=CH2 ГСН; Н Н Br Н- CH3 CH,ОН

Q: H NO2 A) H2C=CHNO2 B) CH;CH-CHNO, C) + H2C-CHNO, D) + H,C-CH2

A:

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: (a) CH,CHCH,CH,CH3 (d) CH3 (b) CH;CHCH,CH,CHCH3 CH3 CH3 (е) (c) CH,(CH,),CHCH,CH3 (f) ČH,CH,

A: For nomenclature  of Alkanes  and cycloalkanes, select the longest carbon chain as parent chain,…

Q: E € (iv) N H HN Η 225°C Pyridine 120°℃ + H₂. +SO3- (0) KMnO4 (O) alc. KMnO4 A?A? ?+ ? 4?-

A: Given,

Q: CH2(COOEt)2 A C,H,ONa OH", H* SOCI, C- PBr3 51. n-C3H17-CH-CH3- ÓH 1. Mg, ether 2. CdCl2 3.…

A: The answer is as follows:

Q: Give an acceptable name for each aldehyde.

A: According to IUPAC rules the name of compounds a) 3-methyl Hexan-1-al b) 3,5-dimethyl heptan-1-al c)…

Q: Br NaCN H3O+ [1] LIAIH4 [2] H₂O A C (CH3CO)₂0 SOCI₂ в - D F CH₂OH, H+ [1] (CH3)2CuLi [2] H₂O [1]…

A: Given are organic reactions.

Q: Draw the products formed in each reaction.

A: Note: Since you have posted a question with multiple subparts, we will solve the first three…

Q: HC=CCH,CH, CH,CH=CHCH, CH3CH2CH2CH3 С. d. HCI, H2O, H2S e. CH3CH2CH3, CICH2CH2OH, CH3CH2OH

A:

Q: 包 週 (iv) ZH N Η HN H 225°C Pyridine 120°C ?A?A? ?+ ? + H₂ +SO3 (0) KMnO4 (0) alc. KMnO4

A:

Q: + 2H2 H20 > B Na H3C-C: EC-CH3 + 1H2 A + Cl2 NH3(1) A H20 → B H2SO4 -c=c-CH3 + H2 Lindlar H,O H3C-C…

A: Hydrogenation is process of adding hydrogen across the unsaturated bond

Q: COH H2SO4 (cat) NaOH HO CH3OH B CH3OH 4. H2SO4 (cat) OCH3 H2SO4 (cat) D+E C H20 H20 NaOH G +H H20…

A:

Q: What is each compound’s systematic name?

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

Q: i. HC/ZnCl2 CH;CH,OH j. HO HCI/ZnCl2 CH3

A:

Q: What is each compound’s systematic name?

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

Q: CH,0 CH, CH-C-a HNO, Fe, HCI AICI H,SO, Pd/H2 Brz FeBr KMNO,

A: Stepwise synthesis is given below

Q: Draw the products of each reaction.

A: The reaction of Chlorobenzene with sodium amide in the presence of liquid ammonia gives Aniline.…

Q: What is each compound’s systematic name?

A:

Q: Write a line-angle formula for each condensed structural formula.

A: The line structure of the molecules given are as follows:

Q: Which of the following compounds has an asymmetric center?

A: Asymmetric centre is a molecule having a special arrangement of ligands which is not superiposable…

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: COH2 H3C H,C-c Br H,C H3C H,C-ce :Br: + H,0 TS = TS = HO: d. CH3 H3C Br :Br: TS = TS =

A:

Q: CHICHCHỊCH, OH CHE CHCHỊCH, -ght OH CH₂- CH3 -C-CHCH₂ CH, OH OH PCI, SOCI₂ HBr HC1, A

A:

Q: d. H3C KMNO4 ОН H3C е. OH CH3 KMNO, f. HI H3C-0–CH2 CH3

A:

Q: What stereoisomers would you expect to obtain from each of the following reactions?

A:

Q: 1- CHy-CH-C-L-CH;(CH2);CH, Zn 2. CHy-CHyCH-CH-CH;-CH, Aceton KOH 3. CH(CH;}«CHz«cCH;CH, Кон 4.…

A: Given: The above organic chemical reactions    To find: The final products

Q: а. CH3 HCI/ZnCl2 . CH3 OH b. HCI/ZnCl2 CH3(CH2),–CHOH C. н он CH;-C-CH–CH; ċ–CH–CH, HC/ZnCl2 ČH,

A: Alcohols undergo substitution reaction with Lucas reagent. Primary alcohols follow SN2 mechanism and…

Q: How will the rate of each of the following SN2 reactions change if it is carried out in a more polar…

A:

Q: What stereoisomers are obtained from each of the following reactions?

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

Q: a. CI (еxcess) H3O* b. .N. H20 С. HO- H3O* エーZ d.

A:

Q: Which reaction in each of the following pairs takes place more rapidly?

A: a. The reaction takes place more rapidly is, Because, CHS- is less solvated by water and sulphur is…

Q: Alkyl halides 1.1 CH3 CI CH,OH A CH3 K' OC(CH,), H3C Figure 1 1.2 CH3 Na OCH,CH, C Br H3C Figure 2

A: Alkyl halides are highly reactive compounds due to the presence of polar carbon-halogen bond in…

Q: d. C,H-C-CH, H* e. C,Hs-C-CH f. C,Hs-C-CH; NaOH g. CH;-C=C-CH, HgSO., 4 h. C.Hs-C-C.H,

A:

Q: a. CH,CNHCH, + H;O* → ? + ? || · CH;CH,CH,C–OH + CH,NH, b. ? + H;O* c. CH,CHCH,CNHCH,CH; + ?…

A:

Q: Br NaCN A H30* SOC2 В 1. → D 2 1. LIAH4 2. H20 CH3OH, H* 1. DIBAH-H F 2. H20 1. LIAH4 2. H20…

A: We have to give the products B, D, F, and J.

Q: В сиз (сиг) зинг D из C CH₂ ((U₂), NV₂ CH=O ↓ a₂ so C MeOH E+3 N Meok Hesou, A

A:

Q: H HH 1 H-C-C-C-H Н Br H 2. CH;CH,CHCICH3 F 3.F. F Н Br H H 4. H-C-C-C-C-CI H H HH 5 CH3CC1,F CI CI…

A: Given that : We have to write the names of the following set of alkyl halides :

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

A:

Q: Which of the following reactions occurs more rapidly?

A: The reaction which occur most rapidly is the reaction in option B as Epoxide is getting formed in…

Q: 1. CH3-6-CH,. G a.60°C_ 1. LIAIH4 -CH2-C-OCH3 2. Н.О 1. CНз-С-сHз, Cl—с-с—CІ, -60°C (h)…

A:

Q: Br CH3 dBr OH a) HO' and C2H5 CH3 C2H5 OH Br b) and Br SCH3 SCH3 c) and Br Br d) and

A:

Q: (e) CH,CICHB1(CH2),C(CH,CH3);

A: IUPAC name : 2-Bromo-1-chloro-7,7-diethylnonane

Q: a) CH3 CH3 NaOH NaBr CH2-C-CH, H3C Br b) CH2 „CH, + HBr + NH, H3C CH2 `NH2 с) CH3 + KCI + KCN CH2-HC…

A:

Q: 1. 2eq CH3M9B 1.LIAIH4 F 2. H+ 2. НаО PBR3 CH30¯ Na + 1. NaBH4 B 2. H2O CH3-CH2-Č-OH C CH3CO,Na |1.…

A:

Q: What is each compound’s systematic name?

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

Q: a. NH2 + HNO2 + HCI b. NH2 + HNO, + HCI CH,CH,CH,CH3 С. CH,CH3 -CH,NH, +HNO, + HCI

A: We have to complete the given reaction as step 2

Q: d) C43- CH -C=c-H ) CiHy - C4-C=C-H Z HC! -> ラ=H>-コ- 1) 03 2) zn /H30+ f) CHエム Zn ( Cu) HBr 2 Li h)

A:

Q: Draw the products of each Sharpless epoxidation.

A:

Q: Cl, КОН A H,O CH CCI, D E F etanol H+ H,SO, Br, CH,-CH,-CH, -ОН — А — 2КОН KMNO, H SO 4c:c H, C D +E…

A: Since you have asked multiple questions, we will solve the first question for you. If you want any…

Stereochemistry and Isomerism

Stereochemistry deals with the three-dimensional structure and properties of molecules. It explains the arrangement of atoms and their manipulation within a molecule in a 3D structure. Stereochemistry can be dealt with all types of molecules. Based on the stereochemistry of a molecule, the physical and chemical properties of the molecules vary.