10. Provide the product and mechanism for the following reactions. | HBr

Q: For the reaction sequence below, select the expected major product. 1) Br2 2) 3 eq. NaNH2/NH3 3) H.O

A: The solution is as follows:

Q: OH OEt 1) 2 PhMgBr Ph Ph Ph 2) H30*

A: Reaction of Ester with Grignard reagent.

Q: ) Provide a reaction mechanism for the following reactions and name the major product for each. HBr…

A: The reaction of alkene and HBr follows markonikoff addition reaction because intermediate…

Q: Provide a detailed step by step mechanism for the formation of the product in the reaction Brm Na H>…

A: NaH is a strong base and will extract hydrogen from a compound. In this compound, Na will be…

Q: 1) 9-BBN 2) H2O2, NaOH

A:

Q: 6.) Provide a reasonable mechanism, including all curvy arrows and intermediates, for the following…

A: Fluroine when attached with aromatic ring becomes a better leaving group. Fluorine is having…

Q: НО. ОН H+

A:

Q: Provide the mechanism for the 4th and final reaction in this synthesis: KMNO4/H+ НО OH

A:

Q: Provide the product and mechanism for the reaction: ОН CrO3, H,SO, H,0

A: This reaction is an example of Jone oxidation. Mechanism of Reaction:

Q: a) CH;CH,0 CH3CH2CH, b) Br NH2 c) Br d) + CH3

A: Note: Ether functional group is produced for parts a and parts b.

Q: 4. Show the detailed mechanism for the following reactions. Label steps (Sn2, protonation..), and…

A: We have given the organic reaction and we have to find the mechanism of the reaction.

Q: CH-CH, CHCI, Show the mechanism step by step to obtain the product

A: We are authorized to answer one question at a time, since you have not mentioned which question you…

Q: 8a) Show the mechanism for the radical reaction of pentene 3-methylhexane with Br2 in the presence…

A:

Q: 6. Provide the reagent/s for the following reactions. Provide a detail mechanism for each reaction.…

A:

Q: (10 points) Complete the reaction scheme below. Show all reagents and intermediates. No reaction is…

A: Ans

Q: Give step-by step Mechanism Give step-by step Mechanism HCI OCH2CI -Br CH3CH2OH Br Br Br2 'Br Br…

A: We have to the step by step mechanism for the following given reactions as follows in step 2:

Q: Provide the mechanism for the 5th and final reaction in this synthesis: OH KMAO4

A: This is an oxidation reaction.  Here secondary alcohol is converyed into ketone using potassium…

Q: В. С. :ÖH H;C ČH3 CH3 ČH3 B.

A: The functional group is a key component of a molecule that furnishes the characteristic chemical…

Q: H2O ? .CI Br2/H2O ?

A: Water is a polar protic solvent and the alkyl halide is tertiary which favours Substitution…

Q: Show the reaction mechanism for the formation of: a. RCONH2 from the reaction of RCOOR’ with NH3

A: given find mechanism of RCONH2 from the reaction of RCOOR’ with NH3

Q: | NH3 + Cr H3C NO2

A: Trans effect can be defined as the ability of ligand to increase the rate of substitution of a…

Q: OH .... HO HO

A: The conversion of alcohol to an aldehyde or carboxylic acid or the conversion of aldehyde to…

Q: 10-Predict the predominant mechanism and draw the major product. Br .? a NAOH Br NaOH b Br NASH DMF…

A:

Q: Show the steps of synthesis (1st semester Orgo).

A: The conversion of one organic compound into others is done by different types of reaction, all these…

Q: 2. Write the conditions/products and mechanisms of the following reactions. ? EtO OEI (a) EtO OEI

A: The reaction go via substitution reaction mechanism. Reactant consists of two acidic proton.

Q: SOC2, py HO:

A: Alcohol reacts with thionyl chloride in the pyridine solvent to give alkyl chloride.

Q: 10 (b) Show all rearrangements that could occur that would result in a more stable carbocation in…

A: Tertiary carbocation is more stable than secondary carbocation which is more stable than primary…

Q: NEN N. +] の☆

A:

Q: 1. t-BUOK,t-BUOH CI 2. HBr Br

A: Tertiary butoxide is a hindered base which on reaction with alkyl halide undergo elimination…

Q: dicate the steps for the transformation HO. HO, → → → H5C6 OH

A:

Q: Select the major organic product of the reaction. NaBH4, MEOH product

A:

Q: Question attached

A: The product of the above reaction is given below,

Q: Br NaOEt ELOH

A:

Q: Br t-BUOK t-BUOH

A:

Q: Find the product by writing down the mechanism of the reactions given below.

A:

Q: 10.2 Complete the following reactions:   Show the step-by-step process. Do not use shortcut methods.…

A:

Q: H;O*

A: In the given reaction the alkene is hydrated to form an alcohol.

Q: H2O Н-ОН b. Br CH;COOH + CH;COOH Br CH3OH Br CH,0° Li + d. CH;OH • H-OCH3 ÓTs е.

A: Strong base  ------>  E2 Weak base --------> E1 Strong nucleophile  ------> SN2 Weak…

Q: excess HBr Br Br

A:

Q: 5. Using curved arrows, showing key intermediates and any formal charges, propose a detailed…

A: Epoxide ring opening can take place in either side of ring which depends on the condition of the…

Q: Complete the following reactions, write major product(s) and specify the mechanism if ; SN1, SN2, E,…

A: We will write the product

Q: 2) Write the major products A- P for each of the following reactions. Br KMNO OH Zn E 1) 03 2) Zn/…

A: The answer is given as follows

Q: b) Describe the type of nucleophilic substitution that occur in the reactions below: i) CH₂COO'Na'…

A:

Q: Which solvent will allow this reaction to occur the most rapidly? NaCN "Br CN DMSO acetone/water…

A: The perfect solven for this subsitution reaction would be DMSO  * DMSO is polar aprotic solvent(THAT…

Q: The following reaction can be carried out in two steps. Choose the correct reagents i) and ii) to…

A:

Q: Show the mechanism of the following reaction. Br HBr Br

A:

Q: 7. Give the mechanism and product for the reaction below. HO. HS0. mechanism:

A: Reaction mechanism helps to give information about the slowest and the fastest step of the reaction.…

Q: 1. Excess LIAIH4 MeO НО 2. H2о

A: Given reaction: We have to write the mechanism of the reaction.

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.