What would be the best synthetic approach for the compound shown in the box? Br KI HNO3 Br2 Sn or Fe NaNO2 A) FeBra HCI H2SO4, H20 H2SO4 B) 12 NANH2 NaNO2 KBr H2SO4, H20 CuBr Felg C) Br2 HNO3 Sn or Fe NaNO2 KI FeBr3 H2SO4 HCI H2SO4, H20 KI D) Br2 NANO2 Sn or Fe HNO3 FeBr3 H2SO4, H20 HCI H2SO4 A В

Q: 1. 1) Hg(OAc)2, H20 2) NABH4 1) Hg(OAc)2, H20 2) NABH4 1) NaNH2 2) CH3CH2B. 3) HgSO4, H2SO4, H20 3.…

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Q: HCN KCN

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Q: Bee: Select the most likely mechanistic explanation for each. A HH HH CH₂CH₂CH ЊCH CH₂CH₂ OH…

A: SN1: Substrate has the tendency to form stable carbocation  There is possibility of rearrangement…

Q: ဝ a) H3NCHCNHCH₂CO₂ CH3 -N=C=S 1) NaOH 2) anhydrous CF3COOH 3) aq HCI HN- H CH3 CI + Hဒ္ဒNCH၇CO2H

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Q: Modify the given copy of the starting material to draw the product. H₂C. Br 1) CH3CI, AICI 2) KMnO4,…

A: The Friedel-Craft alkylation reaction is an electrophilic substitution reaction. Benzene ring on…

Q: Identify the reagents needed for the given reaction. CH2=CH-CH,CHO → CH2=CH-CH2CH2OH Select one: O…

A: Sodium borohydride, NaBH4 is a reducing agent and it can selectively reduce a carbonyl functional in…

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A: Given,

Q: Which of the following mechanistic steps contains an error? Options:   arrows 1   intermediate 2…

A: Alkanes can be halogenated in the presence of light or heat. The alkane does not contain any…

Q: try CH 3 C=C CH 2 CH 3 draw + HCI all excess possible products

A: The above reaction is a addition reaction to     in which HCl is added to it in excess.The reaction…

Q: A B OEt HO. ZI ZI

A: Applying concept of organic synthesis.

Q: Part A Find the suitable reagent for the transformation: H3C OH H3C OH KMnO4, H2SO4 O K2Cr2O7, H2SO4…

A: The objective of the question is to identify the correct reagent that can be used for a specific…

Q: Canvas A Select the reagent combination to successfully execute indicated transformation. ! A) i)…

A: Step 1: Step 2: Step 3: Step 4:

Q: F3C Br2, Fe A HNO3, H2SO4 В NO2 HNO3, H,SO4 Br2, Fe NO2 C HO3S' D H3CO

A: The above given reactions are aromatic  electrophilic substitution reactions, in which benzene ring…

Q: Br 2) Д 3) H2O

A: Alkyl bromide reacts with Mg to give Grignard reagent.  When Grignard reagent is treated with…

Q: 77°F Mostly cloudy Which reaction sequence best accomplishes this transformation? 20 Br₂ EtCl AlBra…

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Q: Please complete the following synthesis. 0-0²- وا Br₂, hv F NBS heat B Br₂, DCM G H₂, Pd Br с HBr,…

A: Given, the synthesis reaction is:

Q: Select the best reagent and conditions for each step of the sequence below: 1. 1. Reagent…

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Q: What reagents would be needed to produce the product shown as the major product? ОН Br A) 1. H2SO4 /…

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Q: ܐ :ÖⓇ CH3 H H ܘ0 Draw Intermediate CH3Br H ܘ X

A: In this reaction base (-OCH3) abstract most acidic hydrogen is attached with carbon next to…

Q: What reagents are required to carry out the following reaction (select all that apply)?     a HNO3 b…

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Q: 2:26 PM Mon Oct 16 d) Same product formed from left and right. Use the other one to verify your…

A: 1) The Friedel-Crafts acylation reaction involves the addition of an acyl group to an aromatic ring.…

Q: Draw the products and necessary reagents of the three step retrosynthetic reaction sequence shown…

A: Nitro group can be reduced with metal based reduction such as Fe/Sn and HCl. HNO3 + H2SO4 (cat.) Is…

Q: 1) NaOCH3 / HOСH OCH3 2) H30 H20 1) (CHз)2CuLi 2) H30©/ H20 (pH = 7) %3D

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Q: Please complete the following synthesis. 1. Li Gilman Ragent + ? 2. Cul Br Br Br Br A B D Br Br Br G…

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

Q: Which starting material is required for the synthesis below? ? 1. 03 2. Me₂S 3. H₂CrO4 4. m-CPBA Me…

A: To identify the correct starting material for the synthesis of CH3​COOCH2​CH2​CH2​OOCCH3​ using the…

Q: What reagents yield the desired product?

A: In this question, we want to select desired route using Reagents to give desired product.  You can…

Q: 3. Which of the following reactions would you expect to form the products of sulfonation shown?…

A: Sulfonation is a reaction in which the -SO3H group is added to the benzene ring. This reaction is…

Q: Macmillan Learning Add two curved arrows to the reactant side to illustrate the movement of…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: CH3 HCI CH3 H3C. H3C. H. но CH3

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Q: Rank the following carbonyls according to their electrophilicity (1 = most) OEt O O xo NEt₂ O CF3 O

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Q: incorrect. NH₂ Br Edit Drawing NO₂ Modify the given copy of the starting material to draw the major…

A: Iron in the presence of acid reduces nitro to amine while having no effect on halogens on the…

Q: Be sure to answer all parts. Draw a stepwise mechanism for the following reaction (be sure to…

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Q: PO-13. Rank from slowest to fastest rate of SN1 substitution. Br Br Br II III (A) I<III <II (В) III…

A: Answer is (D) option

Q: Choose the correct set of reagonts, Circle the correct answer Br CH₂ NO₂ A) HNO3 /H₂SO4 →…

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Q: Name the following organic compounds: compound CH3 I CH₂ I CH₂ -CH- CH,— CH,— CH, CH3 - CH₂ - CH₂ |…

A: IUPAC nomenclature rules for alkanes: 1) find the longest continuous straight carbon chain. 2)…

Q: 1. Br₂ 2. 2 eq NaNH2 3. Na, NH3 A) B) C) D)

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Q: y=& OH g) LAH A CI 1) Naº 1) Mg 2) CO₂ 2) Bri ОН of S I no KOBr NH₂ H3C K₂Cr₂O7 A h) A H* CH3 H3O* B…

A: The above problems are based on the interconversion of functional groups by using wide variety of…

Q: Step 1: NaOCH3   Step 2: Br2   Step 3: 3 eq NaNH2 then H3O+   Step 1: KOtBu   Step 2: Br2   Step 3:…

A: Potassium tert-butoxide is a bulky base and always abstracts proton from the less hindered site…

Q: Which conditions will most efficiently affect the transformation shown? A) NaBH₁, CH;OH B) PCC HO C)…

A: The reduction of carbonyl results in the formation of alcohols. A reducing agent is used for the…

Q: What is the best way to perform the following transformation ? Br- NH2 ?

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Q: 8. a) Consider the following acids: FCH2CO2H CICH2CH2CO₂H || Circle which is the strongest acid?…

A: -&gt; The compound is most acidic if the conjugate base is most stable.

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.