`CI "OH NO2 ÑO2 C OH R. MgBr .R' R. 1. R' `R' 'R' ОН 1. OsO4 2. H2О2, Н2О ОН ОН E A HCI H2O ОН

Q: 1) PhN=C=S; 2) HF CF3CO2H HF 1) DCC; 2) HF NaOH, H2O 1) DCC; 2) CF3CO2H 1) DCC; 2) NaOH PhN=C=S DCC

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Q: HO & HO 8 H 1. H₂NNH₂, EtOH 2. NaOH Zn(Hg), H3O* NaBH, CN, EtOH, pH 5 CrO₂ H₂SO4 H₂O pH 5

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Q: H,SO4 (A) -OH но 180° K,Cr,0,, H,SO4 (B) он (F) (E) (D) (C) \KMNO4, NaOH, Hz0 PCC, pyridine sodl,…

A: Since you have asked a question with multiple sub-parts, we will solve the first three sub-partts…

Q: 14) Al(NO3)3+ Ga > - - Туре: 15) H2SO4 + NH,OH > - Туре: 16) CH3COOH + 02→ Туре:

A: The solution is as follows:

Q: Hg(OAc)2, H,O -CH3 Hg(OAc), H;0 NaBH, BH3 HO2 CH3 THE OH

A: Hello. Since the question contains multiple subparts, the first three subparts are solved. In case…

Q: What are the products of the following reactions?

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

Q: Draw the structures of compounds A–H in the following synthesis scheme.

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Q: HBr/ROOR/hv a) Br NaOCH,/isi b) ? OC2H5 1. LIAIH4 c) 2. H3O* 1. NaOH (aq.) d) HO ? 2. CH3CH2B

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Q: OH HO. OH c) Li AlH, SOCI2 if PCC CH2 C2 d) OH NaBH, ? b) HO H H2CrO U KM.O4, OH2 2) Hg0* 4.1 e)

A: 1st option is given condition is PCC , PCC is selectively to give aldehyde 2nd is stepwise oxidation…

Q: Na SCH,CH, 3 DMF, 0°C CH;I NANO, 5°C CH; CH,-C-OT. CH, H,0 22° С CH3 CH;OH Br 22° С CH, (CHa)»COH,…

A: In E2 elimination , base takes the beta Hydrogen which is anti in stereochemistry with respect to…

Q: Identify compounds A‒M in the following reaction sequence.

A: The reagent "RMgBr" named as "Grignard reagent". This reagent helps in generating…

Q: Identify the major product for each reaction

A: The nucleophilic substitution reaction of organolithium RLi with ester, the alcohol is formed as the…

Q: CHO H-OH H-OH CH₂OH 1. NaCN/HCI 2. H₂/Pd/BaSO4 3. H₂O/H

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Q: + HBr ROOR H₂O H₂SO4 H₂0 H₂SO4 H₂SO4 1) BH3 2) H₂O₂/NaOH 2 Br₂ 2 HCI 1) Hg(0Ac)2, H₂O 2) NaBH4 1)…

A: Fill in the blanks with appropriate structures to identify the major product of the reaction.

Q: 3 Fe(s) + 4 CO2(g)  -------Fe3O4(s) + 4 CO(g) Keq =   . (b) Fe2O3(s) + 6 HCl(g)  ------2…

A: To solve this problem we have to write the equilibrium expression of given equations .    Note : In…

Q: HO EtOH, H₂SO4 cat, A 1. NaOEt, wwwmme EtOH Et o OEt 2. H3O+ H3O+, A 1. NaOEt 2. 3. NaOEt Br

A: In crossed Claisen condensation reaction one of the molecules is an enolizable ester reacts with a…

Q: Eto OEt H30*, A P NaOEt, EtOH CN Q NaOEt, ELOH H30*, A NC R H.

A: Both reaction involves the three common steps  i) Generation of carbanion ii) Attack at carbonyl…

Q: 1. Os0, pyr н но 2. NaHSO,(aq) ÓH ČH3 Br, NaOH H,0 CH 1. BD,, THF но 2. H,0, OH- ČH3 CH3 Br, н но…

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Q: cetie aeid NO. OH KC0, ON AIC OH NaOH DMSO, 00°C NO, OH -N," or OH 2 C4 acetic acid

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Q: 1) ВНз, THF (b) H20 2) HаО2, NaOH, НаО cat. H2SO4 Br2 Ph Ph 1) Hg(O2CCH3)2, THF/H;O (d) 2) NABD4 (e)…

A: Applying concept of organic synthesis and reagent.

Q: Br HO EtO₂C CO₂Et C5H11 NaOEt / EtOH 99% CO₂Et H₂/Pd-C C5H11 8 OH Br 10 OH EtOH 72% HO NaOH HO OH 11…

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Q: CH2(CO,Et)2 R. COOH II RCH(CO,Et)2 R. COOH III ACCH,CO,Et R. COCH3 IV RCH,COCH; R. COOH R. .COOH V…

A: Decarboxylation is reaction in which carboxyl group is removed with the emission of CO2.

Q: EtO NaOEt, E1OH H NaOEt, E1OH EtO H NaOEt, E1OH N2OET, E1OH Eto I OEt

A: All reactions are condensation reactions. All involves common steps  i) Generation of Carbanion ii)…

Q: OH 1. ? OMe 2. ? a. 1. MsCI, pyridine; 2. NaOCH3, CH3OH b. 1. HCI, pyridine; 2. NaOCH3, CH3OH c. 1.…

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Q: CH,COH H;SO, CH, KCr,O, CH;COOH H;SO, K.Cr,O, CH CHOH

A: Balance Chemical equation means no of atoms should be equaal in both side reactant and product

Q: H20, H2SO4 (i) HBSO4 1. Оз, СН-Clz (ii) CHCH,CH3 2. Zn, CH;COOH, -78°C CH,I, (iii) Zn-(Cu), ether 1.…

A: We are authorized to answer three subparts at a time, since you have not mentioned which part you…

Q: HNO, (1 eq.) H2SO, Br 0 °C NO2 HNO, (1 eq.) H2SO, 0 °C он

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Q: 1)A PBra 1) Mg он но NazCr2O7 HSO, H2O HOV K ко 2) H20 ÓH Br (H2SO.] 2) || -H,O H. 3) H:0 Mg BrMg…

A: For the synthesis of first product, CH3CH2Br is appropriate reactant because when it react with Mg…

Q: CH;OH CH3 22° С `Br KBC(CH3); (CH),CОН, 82° С

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Q: ooredoo O0: 73 10:37 PM H3C-H,C i) + Ph;P=CH-CH3 ii) (CH3),CHCH,Cl AICl3 ii1) H,SO4 OH CH3 H* iv)…

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Q: 1.03, CH2C12 2.Zn, НOАс b. 1. HgOAC)2, H,0 2.N ABH4 CH=CH2 Ch H2O

A: The reactions that involving organic compounds are known as organic reactions.  Alkenes are the…

Q: а. NaOH + HC1→ NaCl + H2O b. Pb2+ + 2C - PbCl2 с. AGNO; + HC1 → HNO3 + AgCi d. 2HC2H;O2 + Ca(OH)2 →…

A: Redox reaction

Q: (a! CH3 CO2H (b) CH3 1. Cl2. FeCla 2 KMnO4 1. HNO H2SO, 2. CH3CL AICly 3. Fe. H0 4. NaOH, H,0 NH2…

A: In organic conversion, suitable reagent converts the reactants into products. Reagents react with…

Q: NH₂ NO₂ Br NH₂ NH₂ 1) (CH3)2NH/H 2) 3) H3O 1) Fe/H3O 2) NaOH H NaBH3CN 1) CI 2) HNO3 / H₂SO4 3)…

A:

Q: What are the final products for these reactions? *mechanisms not necessary

A: The final products of the given reactions can be written as : The reaction of alkyl halide with KCN…

Q: (2a) 2 HCI (aq) + Mg (s)- MgCl2 (aq) + H2 (g) 1) (2c) HC2H3O2 (aq) + NaHCO3 (s) → NaC2H3O2 (aq) +…

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Q: 1. NaOMe 2. H3O* Br2, H20 NaOH (dil.) H2SO4, H2O

A: According to our guidelines, Since you have asked multiple reactions, we will solve the first three…

Q: (A.H) RCONCS CH,CONCS NH2 'R M.w=(63.20 H. ELOH M.W: M.W: 303.75 g: 1.8325

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Q: Br NaOCH,2 MeOH Br Br NaOCH, MeOH, 78°C NH(CH3)2 OTs DMF H3C NaOH MEOH, 82 °C

A: The products of the following reaction are :

Q: __ Al2(SO4)3    +     ____ H(OH)  ?  ____ Al(OH)3   +     ___ H2(SO4)

A: Aluminium sulphate is a salt of strong acid (sulphuric acid) and strong base (aluminium hydroxide).…

Q: NABH4, A но HO, ethanol OH OH [1] LİAIH4 HO, [2] H2O OH OH Ag20, H2O NHẠOH, ethanol HO,

A: First two (that is NaBH4, Ethanol and LiAlH4, H2O) are the reducing reagents. And the third reagent…

Q: Br Me A CN NH₂ 1. Br2, FeBr3 2. BrMgCH₂CH₂CH3, THF; aq. HCI 3. NaBH, MeOH 4. NaH, Mel, DMF Br B OMe…

A:

Q: Br 1. Mg, ether 2. Со2 (a) 3. Н.О, Н OH H+ (b) HO, (с) NaHCO3 HO. ? HO. CI (d) K*OH (e) HO, 1. NaCN…

A: We have to provide the product or reagent for the following given transformations as follows in step…

Q: i) H. .CO2H 150°C ? + H20 90% H `CO,H Maleic acid ii) (CH;CO),O + (CH3)½C-OH ÇOOCH3 i11) + OH NAOH ?…

A:

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

A: a. The H+ present in HCl attacks C with one H present in C=C and forms stable tertiary carbo cation.…

Q: (r) H* + CH;CH2OH H2NNH2, OH (w) Нeat 1. Br2, FeBr3 (х) 2. Mg, Et20 3. 4. Hзо*

A: The major products of the following reactions are as follows:

Q: ca) CI (CH2=CH)2CuLi ether, -78° C (9) 1. 2 CH3CH2CH2MgBr, ether CI 2. H;0* (C) who 1. 2 H3C- -MgBr…

A: In acyl substitution reaction, nucleophile can always attack on electrophilic carbonyl centre and…

Q: Can you help me solve this?

A:

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.