Select the major organic product resulting from the sequence of the reactions written. CH3 Zn(Hg) AICI3 HCI CH, CH3 CH,CH2C H,CH, CH3 CH CH,CH CH-CH,CH; CH(CH3)2 2 4 0 1 O 2 O 3

Q: 2) Give the IUPAC name for the major product of the reactic CH3 C-C-OH HC) CH3

A: 3° alcohol in presence of HX(X=Halogen) undergo substitution reaction to give an alkyl halide.  In…

Q: Identify the specific type of chemical reaction shown in the equation below CH,CH,OH + 30, → 2C0, +…

A:

Q: 2. Write the products formed as a result of the reactions given below. NO2 H „N H,N a) HC CH3 + NO2…

A: Write the product formed as a result of the reactions given below. (a) (b)

Q: Name the following compound according to the IUPAC nomenclature: OH OH OH O…

A:

Q: 2) Fill in the missing Reactants, Reagents, b) НО CH₂OH OH OH ОН H2 cat Pd/C H2O Cu²+ Benedict's…

A:

Q: The reaction of CH - CH = CH - CH with HOH would form 3. .

A: The alkenes show addition reaction because of the presence of double bond, The addition takes place…

Q: Draw the product(s) for the following reaction.

A: The given reactant is a triester. It reacts with sodium hydroxide (NaOH) resulting in the formation…

Q: ra mple 2,13 regioselectivity of the reaction of Br, with alkanes. CH3 → Monobromoalkanes + HBr heat…

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Q: Modify the given structure to show the product of the hydrogenation of cis‑2‑pentene. Include all…

A:

Q: Choose the reaction conditions to complete the acid-base reaction shown. H C:O Q B NaNha hexane…

A: The reaction of a terminal alkyne with NaNH2 (sodium amide) in hexane is often employed in organic…

Q: 2. Give the product(s) of the following reaction: H₂C-CH₂ CH₂ CH₂-CH₂ 1 CH CH₂ + NaOH

A: The objective of the question is to find the products of the given reaction in which substituted…

Q: 2. Write in the products of these reactions: a) ABr NaOH CH3 SN 2 b) NaOCH, CH;CH2CH2I c) (S)…

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Q: H -S no 16.pan NaOH H₂O Br

A: This is an example of thiozolium salt catalysed benzoin condensation

Q: Write the products formed as a result of the reactions given below. NO2 H N. H2N a) H,C- `CH3 NO2 b)…

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Q: A. Assign the IUPAC name and the common name of the following organic compounds: 46. CH3 CH; —Ҫ—SH…

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Q: .S. H2SO4 (k) CH3 Na2Cr207 (1) Heat `C(CH3)3 :S:

A: We have to draw the structural formula for the major product(s) resulting from the following…

Q: Draw structural formulas for the products of the reaction shown below. CH3CH₂-O-CHCH3 + HBr CH3

A: The given reaction has ether and hydrogen bromide as reactants. Ether cleaves in presence of HBr to…

Q: Н OH2 H он, H + H2O +

A: In this step, H2O acts as a base. As a base, it abstracts a proton from the reacatnt.

Q: Which of the following secondary alcohols can be prepared by the reaction of methyl formate with…

A: The Grignard reagent is responsible for the addition of two equivalent substituent at the carbon of…

Q: Complete the following reactions and use IUPAC method to name the product

A: •Here in given reaction alkene is reacting with H2/Ni. •Here is the reaction:-

Q: Where does the 40% and 60% product come from? How to determine this?

A:

Q: 22) Draw the structure of the product of the following condensation reactions.

A: Given that,

Q: Predict the products of this organic reaction: CH3—CH2−C−NH–CH2–C—CH3 + H₂O + HCI ?

A: Given an amide, water and HCl.Draw the product  of reaction.

Q: H3C-C=C-CH2-CH-CH3 2 mol Br2 ČH3 H3C-C=C-CH2-CH-CH3 + 2 mol HCl ČH3 H3C-C=C-CH2-CH-CH3 + excess H2…

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Q: Br. ОН CH3 CH3 H3C ОН H*, remove water Br. CH3 H3C CH3 1) Mg/ether 2) CH,CH=O 3) H2O+

A: Please go through my hand written notes for the solution.

Q: What reducing agents should be used to obtain the desired target molecules?

A: The catalytic hydrogenation of but-2-enal in the presence of palladium catalyst forms butanal…

Q: Account for the fact that addition of HCI to 1-bromopropene gives exclusively…

A: The reaction between addition of hydrocholoric acid to 1- bromopene is discussed as follows,

Q: H* a) CH,COOH H,C H20 b) CHy-C-H CHy-CH-CH2MGB. H* NABH,

A:

Q: о он OH NaOH CH;CCH,Ċ(CH3)2

A: The reaction taking place is given as,

Q: OH CrO3, H2SO4 H. acetone YZA AZY

A: The reaction given is,

Q: 21) Give the products of the following reaction. CH3 HN H3C `H + CH3 H3C ČH3 H3C°

A:

Q: The carbocation in the reaction act as electrophile) CH3 ___ CH;-C+ CH; (acid, base, nucleophile,…

A:

Q: MA, MD, ME, and MG are ionic compounds in which M is a metal. A, D, E, and G are monovalent…

A: The amount of energy that gets released when two ions combine with each-other to form a compound. It…

Q: CN NO₂ H₂/Pd ? Major Organic Product

A: H2,Pd is used as a reagent in metal catalyzed hydrogenation.Generally, H2,, H2, Pd reduces double…

Q: Select the product of the following reaction: H3C CH2 CH3 "H ТОН 1. p-TosCI, pyr 2. CH,CH,O® Na®

A: Alcohol can be converted into an ether by a nucleophilic substitution reaction mechanism. In the…

Q: Show how to bring about each step in this synthesis of the herbicide propranil. CI CI CI CI CI CI 4…

A: Propranil is a widely used herbicide with molar mass 18.08 g/mol.  It can be synthesized from…

Q: What type of reaction is occurring Ester O H CH₂-C N- H+ HOH + HCI O CH₂-C 0 H 11 CH–CH,-C-NCH, +…

A: #1: What type of reaction is occurring: #(a): The reactant is an amide (R-CONH2).

Q: + Cl₂ dichloromethane, + Br₂ Ho ܗܘ ܐ

A: According to Bartleby Q&A guidelines we are supposed to answer only first three sub parts of…

Q: show-all-working-explaining-detailly-each-step

A: A. C6H5CH2CH3 Compound give Electrophilic aromatic substitution reaction because Benzene ring have…

Q: OH HO CH₂ 8...- + HCI- á CN Cl₂ AICI, N AICI, CI OH C-CH3 -MgBr H+ (two products) heat

A: According to the bartleby guidelines for the multipart questions, I can solve only first three…

Q: CH, но сн, CH;O `CH3

A: Reduction is the addition of a hydrogen atom to each end of the carbon-oxygen double bond to form an…

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.