o-CH3 Ht C-H С-н + H20 ó-CH3

Q: Which molecule can loose a hydrogen and become a nucleophile? Select one: a. H3C– ECH b. H;C- -CH3…

A: The terminal alkynes or 1-alkynes are weak acids and loose a hydrogen when treated with strong base…

Q: 5. For each reaction below, choose the reagent/s A) Br H20 A Br NaOH THF C) KOLBU CI KOTBU

A: The question is based on the concept of organic reactions.   we have to identify the Product formed…

Q: What is the main product of the E2-elimination reaction shown in the box? Br C,Hg C-C-CHs H CH3…

A: Given : Reaction of Structure Containing Bromine group with CH3CH2ONa To find : Product by E2 -…

Q: Which product is formed in the reaction shown below. Click on a letter A to D to answer. HOz CH-COOH…

A: Epoxidation is the reaction where it converts the C=C into oxiranes (epoxides). A variety of…

Q: Draw the major product of the following reaction

A:

Q: 1. Draw the structure of the intermediate products in the following reactions: (C,Hz)jP-CH CH3 AICI,…

A: Steps: Friedel-Crafts acylation Wittig reaction Addition of HBr to alkene Elimination Nucleophilic…

Q: H3C CH3 CH3 Ph CH3 Br ? CH3 t-BUOH

A:

Q: Draw the structure for the transition state in each reaction. а. OH2 H20 b. HO, -OH H20

A: Each chemical transformation passes through an unstable and not isolable structure called the…

Q: 5. Propose an arrow-pushing mechanism for the reactions shown below. а. H2SO4 OH heat

A: a) Reaction is a dehydration of alcohol in which the alcohols are converted to alkenes, the…

Q: [1] For each given reaction, draw the product(s) of nucleophilic substitution and a complete…

A: Given reactions are example of nucleophilic substitution reaction.

Q: OCH3 C-H C–H + H,O + ? OCH3

A:

Q: Provide the ame reaction associated with each reaction below: R-CO-CH3 + N2H/HO" -> Ph-CH2.CH3 Ans…

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

Q: What is most likely the first step of this reaction's mechanism? CH CH;CH,OH Br CH3 Br CH;CH2O- CH3…

A:

Q: Draw the intermediate and final product formed in the following reaction sequence. H30+ HO OH HgSO4…

A: Please note- As per our company guidelines we are supposed to answer only one question. Kindly…

Q: H" HC-C-o-CH,CH3 H,0 j. H о-н + H3C

A: Esters when heated in water in the presence of acid undergo acid catalyzed hydrolysis to produce…

Q: What is the product of the following two-step reaction sequence? Br2 Na CH3C=CCH3 NH3 H CH3 H2N, H3C…

A:

Q: A set of three nucleophilic displacement reactions is shown below: CH3 SOH CH3CH2CCH3 SN1 reaction…

A: The replacement of any atom or group of atoms by a nucleophile is termed as nucleophilic…

Q: 7. Which of (a)-(d) is least likely as an intermediate or product in the following reaction? cat. H*…

A: Reaction of aldehydes and ketones with hydroxylamine (HONH2) gives oximes.

Q: Br CH;OK a) b) Sn1 Sn2 c) d) E1 E2

A: Generally, alkyl halide or alcohols undergo elimination reaction which give rise to alkene.…

Q: Which pair of reactants is most likely to undergo an E1 reaction? O CH3SNa + (CH3)2CHCH₂CH₂CH₂Br at…

A: E1 (unimolecular elimination) is a reaction where there is a loss of the leaving group followed by…

Q: H2OH HO-C- Но- H-OH + HO-C- H.OH но-с-с

A: Esterification reaction in which ester is formed

Q: Draw the major product(s) for the following reaction. H;C O3(-78°C) CH, (CH3)2S

A:

Q: Which compound is the major product of the reaction sequence shown below? O. (1) PCC/CH;Ch (2) H,SO…

A: We have given that  Which compound is the major product of the reaction sequence shown below ?

Q: CH3 SOH CH;CH,CCH3 SN1 reaction Br A, SOH = 100% CH3OH %3D B, SOH = 33% CH3OH, 67% H20 C, SOH = 67%…

A:

Q: H,C 8 CH3 CH,O° H,C CH;OH CH3

A: An epoxide ring is a heterocyclic ring formed by two carbon and one oxygen. Due to angle strain, the…

Q: Consider the following sequence of reaction, Acetone H2SO4 BRCH,COOEt -Zn, HO* Heat If X is a major…

A:

Q: 7. Draw the intermediate and final product formed in the following reaction sequence. MgBr -c-c H…

A: Please find your solution below : 7. Epoxides also known as cyclic ethers on reaction with ethanol…

Q: Arrange the reactants from fastest to slowest in an S№2 reaction. (CH3)2C(CI)CH3 CH3CH(CI)CH2CH3…

A:

Q: Select the product for the following reaction HCI H. + 2CH;CH,OH H3CH2CO, LOCH;CH3 LOCH2CH3 Но. H.…

A:

Q: 1. 9-BBN 2. Н2О2/NaOH 9-BBN %3D -BH 3. H*/H2O

A: Organoborane reaction mechanism

Q: What will be the major product of the shown E2 reaction: CH3 H3C-C-o CH3 acetonitrile H. Br…

A: The elimination reaction E2 is a bimolecular elimination, which has only one step. A new bond is…

Q: 1. NaOCH3 H3C CH3 2. H,0+ CH3

A:

Q: Complete the followsing reactionse a. CH20H + CH3CH2-ott Ho Cit2OH CHO otH +Cu+ CH20H CH3 + ClHz CH…

A:

Q: 14) Draw the correct product for the reaction below. Pd-C/H,

A:

Q: (a) Arrango the tollowing intermediate in order of decreasing stability. Justity your answer. CH…

A: Here we have to write the decreasing order stability of the following given carbon free radical…

Q: I-O0 I Complete the curved arrow mechanism for this reaction: H H HO. HO. HO. ОН MeOH Me H. Me Me Me…

A: arrow is shown from filled orbital to unfilled orbital.

Q: Which of the following steps, if any, are incorrect in the mechanism shown below? "CI COH2 H* CI LOH…

A: The above mechanism is SN1 mechanism, in which the leaving group leaves and stable carbonation is…

Q: The major product of the following reaction is: CH;CH2S Na CH;CHCH,CH,Br CH3 DMSO CH;C=CHCH3 CH,…

A: The nucleophilicity of the given thiolate anion (CH3CH2S-) is higher as the polarizibility of sulfur…

Q: Which reaction will NOT produce a ketone? HS0, H20 HgSo 1) BH THF 2) HO NaOH A. С. 1) BH THF 2)…

A: ->In BH3 nucleophile is H- hence, H- added to that carbon which has less hydrogen.

Q: What is the CORRECT product A for the following reaction? „Br_ i. Mg, Et,O ii. CO2 ii. H,O* i. LIAH,…

A:

Q: Which compound is the dominant product in the reaction shown below? KMNO4 .COOH (A) H*/H,O (B) COOH…

A: In presence of KMnO4, side chain of benzene is  getting oxidised to form carboxylic acid.

Q: Give the major product(s) of the following reaction. MSCI heat CH3CH,OH pyridine CH;CH, O-S-OH…

A:

Q: Provide the missing reagent for the below reaction: Br Br CH CH3 2 eg HBr O Br leg HBr 2 eg Brg

A: Correct answer is 2 eq HBr.

Q: 1. NaOEt CaH12O2 OEt 2. H3O*

A: To

Q: What Is the starting materlal of this reaction? Click on a letter A through D to answer. CH3OH H+…

A:

Q: Which compound is the major product of the reaction shown? H9SO, OH A H2SO,/H2O Он D -HO- Compound A…

A:

Q: 6- Complete the mechanism of the following reaction? HO TSOH, OH + H20

A: The given reaction is an acid-catalyzed cyclic ketal formation. The resulted ketal is a spirocyclic…

Q: CH3-Br Ag,0 C5H13N N(CH3)3 H20 (heat) (еxcess)

A: Interpretation - To write the reactant in the following reaction sequence which is given as above in…

Q: H, CH3C=CHCH,CH,CHCH,CH,OH Pt CH3 CH3

A: Ans  Reaction is metal catalyst hydrogenation to produce alkane

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.