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

Q: CH₂ H -9 10 C OCH, step 1 CH, Ge Ch step 2 CH₂-C C step 3 orts CH,OH

A: To answer : Three curly arrows to complete the given mechanism Type of reaction involved Role of…

Q: 8. H2N-NH- 9. CH3 RČOOH 10. 1. NaBH4 2. H20

A: Given reactions: We have to find the products of the reactions.

Q: H2SO4 a. Alcohol CH3-CH=C-CH3 180°C ČH3 b. Alcohol H,SO4 → CH3-CH=CH2 180°C c. Alcohol H2SO4 →…

A: The species alkene is generated through the alcohol dehydration in the sight of the sulphuric acid…

Q: CI. „CH2CI NaOH H2O SN2 E2 mixture of SN1 and E1 CH3 CH;OH `CH3 >

A:

Q: H3C OH Əcetic acid Hz SO4> alcönol e Hz SO4> H3C ÒH HO acetic acid alconol

A:

Q: NaOH t-BUOK (c)

A: Given alkyl halide is a tertiary alkyl halide. NaOH is a strong base and it is not bulky. Hence it…

Q: H* H3C O-H + H3C.

A:

Q: CH3CH2CI + NaOH KMNO4 CH3CHO KMNO4 в

A:

Q: Arrange the compounds by boiling point

A:

Q: CH3 CH3 H3C H3C HBr `CH3 CH;COOH ОН

A:

Q: H2O5% 5% 5% NaOH NaHСОЗ НСІ i H2SO4 Hexane i i i i Acetophenonei Isopropanol i Ethyl acetate i…

A: Given To find the solubility of organic solvents in 5% of NaHCO3.

Q: NaOH, H20 Cl CH2OH ÇO,H ÇO,H ÇO.H C) D) B) A) Cl HO, Cl CH2ONA ČH2OH CH,OH ČO,H

A: ->NaOH is base hence, it can abstract most acidic hydrogen present in the given compound.

Q: CH,CH,CH,CH,CH.CH,OH b CH,CH,CHCH,CH,CH, OH сH, Br CH,C-CCH, 1. OH Br CH, OH CH,CH-CHCH,CH,

A: Alcohol is a important functional group in organic chemistry. It has a hydroxy group (-OH). Alcohols…

Q: NaOH H20 NaOH + H20 O:

A: The given reaction is the aldol condensation reaction in which two molecules of same aldehyde or…

Q: 1.NANH:/liquid NH2/-78°C 1.NANH:/liquid NH:/-78°C A( C3H16) B(C19H36) H-CEC-H 2.1- Bromo-5-methyl…

A:

Q: CH30- CH;OH

A: Given: The structures of reactants appear as follows:

Q: 1. NANH2; 2. CH;CH,CHO; 3. H*(quenching); 4. H/Pd/BaSO,/pyridine; 5. OsO,/H,O2 H =-H он OH он он Но…

A:

Q: .O-H O-H NaHCO3 (exceso) + H;CO3 H20 O-H I. LO Na I. O-H

A: Given :  To find the products for the given reaction.

Q: H. 1) LAH 2) H,C 1) LAH 2) H,0 (a) (b) NABH, MEOH ? H. 1) LAH

A:

Q: CH3 OH CI-Br + H20 CH3 OH CI-Br + H20 CH3 Br OH + C-Br + H20 CH, CH-Br + H20 но Br CH3 CI OH CI-Br +…

A: The retrosynthesis is the way of breaking up the molecule in mind in such a way so that it can give…

Q: Fill in each box with the appropriate reagent:

A: To write the appropriate reagent for the given reactions

Q: CH H;C CH; CH, CH,OH (3) `CH3 Vitamin A OH (4) OCH,CH, Ramipril IZ

A: Given: structures of vitamin A and Ramipril To find: Different functional group present in the…

Q: OH OH (1) NaOH - (x) (2) H® Reactant x is : 7. (a) CH3CI (b) CH 2C12 (c) CHCI3 (d) CCl 4

A: Given reactant is phenol and product is salicylaldehyde. This is Reimer-Tiemann reaction.

Q: C. 2. Acetone H C H. H H H H H. C H. Pentane C H H. H. H. H. H H. H. 3 H. Methylamine N. H. H.…

A: SOLUTION: Step 1: The order of elution will depend on the binding capacity of the compound to the…

Q: CH3 CH2-CH2-CH3 KMNO4. н', heat CH3 -CH2-CH3 CH CH2-CH3 (а) (b) CH3 COOH HOOC, .COOH CH .COOH (с)…

A: The presence of KMnO4 in presence of hydrogen ion and heat is a very strong oxidising agent. It…

Q: Br NaOH -> ace tone 11 CH3

A:

Q: H2O H2SO4 NH

A: Acetals are geminal-diether derivatives of aldehydes or ketones, formed by reaction with two…

Q: NHt CH3(cH2),CtcI -> ethanol

A: Given that : We have to predict the products of the following reaction :

Q: Based on the following structural formulas, calculate thepercentage of carbon by mass present in…

A:

Q: ? NaOH t-BUOK (c) (d)

A:

Q: LOH 1. NaOH 2. CH;CH2B H2 C0-CH3 H2 HBr o-CH2 CH heat, 250 °C CH2 HCI H3C, Ether

A:

Q: CH:COCH Ph:P = C - (CeH:)2 ethanol Na metal (10) CH:CH:Br QNa (11)

A:

Q: NaOH H20 heat

A:

Q: OH H2SO4 D. E1 E2 heat OH 1.TSCI, pyridine E. E1 E2 2. NaH

A: Elimination occurs when Alcohols treated with concentrated  sulfuric Acid.

Q: НО. НО. 0 Br Br N₁ PPh3 адн 해 :PPh acetone я Н Н NaOH НО 0 но. A 0 PPh₂ В

A: Triphenylphosphine is a weak base, due to the presence of three electron withdrawing phenyl groups…

Q: how it happens? H3C H3C H3C H3C N OH H3C HO- H3C- H3C OH CH3 M9CI H3C H2C

A: Here we have to synthesize the following given compounds through multistep reactions.

Q: 1) Hg(OAc)2, H20 2) NABH CCI4 (an inert solvent) CH3 Cl D. H2, Pd/C ELOH H,ŠO (cat.) CH;OH

A: In the given reactant,  the functional group is alkene. Alkene reacts with various reagent because…

Q: Н до GB3 EtOH Br H H Br H Br

A: In the given problem we need to fill up the table that comprise of the excess or waste data for the…

Q: EtO₂C .CO₂Et Br CHO NaOEt EtO₂C EtO₂C CHO

A: Here we have to synthesize  the following given  target compound  from the given starting material…

Q: 1. NaOCH2CH3 2. H30* O. CH;CH2OH

A: Given : structure

Q: 1) Н—С—-Н 2) CH2 3) 4) 5) 6) он На, Pt NANH2 HаОг, NaOH, H0 CH;Br H2, Lindlar's catalyst CrOз,…

A: The reactions involved in the conversion of ethyne to pentene is shown below :

Q: COOH .COOH COOH d) НООС- f) HOOC COOH COOH HOOC

A: The organic compounds are named according to the rules and recommendation of IUPAC. The names…

Q: (10j) SOCII2 ÒH ру CI CI thionyl chloride (SOCI2) pyridine (ру)

A:

Q: Cl- 1. AICI3 CH2CI2 (solvent) 2. CH:NH, 0: 3. NABH4 MEOH (solvent) Cl Cl

A: These are the examples of intramolecular Friedel-Crafts acylation followed by reductive amination.

Q: Peacciones presentadas siguen el mecanismo SN1 o SN2. 1 H3C CH,01 CH,OH CH CH,COO-1 H3C Br CH,COOH…

A: SN2 preferred primary alkyl halide to give nucleophilic substitution reaction while tertiary alkyl…

Q: 1. NaOEt Rxn I 2. Нао CH3OH cat. H* Rxn II

A:

Q: CH, CH Mg co2 H;O*/H,0 CH,CH,Br diethyl ether KMno4 H3O* /H;O -CH,CH3 KOH / H,0 KCr,07 IV -CH2OH…

A:

Q: 0 CEN | H H HC-C=c-c-c-c-OH | H3C go-de Ha Ho -o-c-c-cooH

A: The International Union of Pure and Applied Chemistry (IUPAC) nomenclature of organic chemistry is a…

Q: 1) (CHa),SICI / NEL CH 2) CH జ 1) 2) CH,CHICO,CH,CH, 3) H;0 (warm) 1) LINPI2 (LDA) /-78°C e) / 15…

A: We have to givemajor product of the following given reactions as follows in step 2:

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.