Draw the products and necessary reagents of the three step retrosynthetic reaction sequence shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore inorganic byproducts. Br NH₂ 1. NaBH4 D 2. H₂O 11 Br2 FeBr3 Br HNO3 NO₂ cat. H₂SO4 Select to Draw

Q: H-C-H 2 O sp² sp 3 sp 32 O sp'd O spºd 3 :ד 3 sp d 3 sp 2 sp sp H 32 sp d -I H :F: :ד: H—N—H 2 sp sp…

A: It is very clear from the options given in the question image that we have to find the hybridization…

Q: a. 1) NaOMe (equiv) 2) CH3CH₂Br 3) NaOMe (equiv) 4) CH3CH2CH2Br HO 1) 2, NaOH 2) H+, HO H+, H₂O heat

A: Shown below is the completed route for the given synthesis.Step 1: Claisen condensation of an ester…

Q: Which in the most basic of the following numbers CONH (2) NHCH CH NH, AC) B(2) CO) D the same OAA…

A:

Q: 'H 1. CH3CCMgBr 2. H3O+

A:

Q: d) e) f) Br 1- 2- Ph H* I Br 3- H¹, H₂O NaOEt EtOH 1. PhMgBr (excess) 2. H3O* 1-03, CH₂Cl2, -78 °C…

A:

Q: Q: Arrange the tollowing Compound, in arder of inerausring Energy? HEH H H. H. 2) (3) C4) A) 1> 2…

A: In Compound 1, both bulky groups are in eclipsed position, hence it is highly destabilised or higher…

Q: Identify the reagents you would use to achieve each of the following transformations. OH с D OH A B…

A: These  Reaction involve ozonolysis  reduction ,protection and deprotection.

Q: Pls help ASAP. Pls do all 4 i beg

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Q: F. Build each of the molecules (a, b, c and d) drawn below (team/group work)__ Br Br Br Br b) C) d)…

A: Since you have posted a question with multiple sub-parts, we will solve first three sub-parts for…

Q: 1.) 2.) CH3Br NH 3.) H3O*, H20 molecular seives (i.e. - H2O) a) 1.) b.) 1.) c) 1.) H. H. 2) 2) 2)…

A: Correct option is (a)

Q: What is the rank of stability of the following compounds in a 1 mol/L NaOH solution? H,CO H3CO OCH3…

A: The answer is as follows:

Q: What is the relationship between: a. I and II? III and IV? b. I and IV? II and IV? c. I and III? II…

A: The molecules with the same molecular formula but different structures are known as isomers. If the…

Q: 1. Hg(OAc)2, H,O 2. NaBH4 1. Hg(OAc), H,о 2. NaBH4 1. Hg(OAc)2, H,O 2. NaBH4

A:

Q: Pls help ASAP on all pls i beg.

A: To solve this problem we have to identify the given compound .

Q: NH2 H. a S -N- HO HO. O A:R, B:S A:S, B:R A:R, B:R A:S, B:S IZ

A:

Q: Choose the correct reagent(s) for the following conversions. Br A B Reagents options: a. HBr b.…

A: HBr adds to Alkenes according to Markovnikov rule.HBr in presence of peroxide adds to alkene…

Q: (d) (e) (f) 00 CH₂Cl2 1. CH3MgBr 2. H3O* HCN KCN catalyst

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

Q: e) f) 1) HBr 2) Mg°, ether 3) CO₂ Na2Cr2O7 H3O+ -NH2 cat. H2SO4 H 1) LiAlH4 2) H₂O 1) SOCI₂ 2) Син…

A: The question is based on organic reactions.We need to identify the product and explain its…

Q: hydrogen by the resonance and the inductive mechanisms. a = acceptor d = donor n = no effect 1. -NO2…

A: The objective of the question is to determine the inductive and resonance effects of the given…

Q: 7 Best reuyent choice ? -> Br oHa Pd ) Fe, HyO", 2) NuOHL

A: Since you have posted multiple questions, we will solve only first question for you. If you want any…

Q: C. Skeletal and Name: * ** H Н-с-н HHH H H H а. Н-с-с-с-с-с-с-с-с-с-н H HH H HH H H H…

A: 1. Select the principle carbon chain 2. Numbering 3. Naming (prefix + word root + suffix)

Q: Problem 9. (1) Na oH (2) CHzI Problem 10. LiAl Ht

A: When carboxylic acid react with base then, base will abstract a proton from the carboxylic acid.

Q: p2 CICO CIĊO Cle 2 Cl,CO + Cl·

A: Slow step is rate determining step. To take slow step as elementary step, we can write rate law,…

Q: H. H. O 1= sp3, 2 = sp3, 3 = sp3 O 1 = sp2, 2 = sp3, 3 = sp2 1 3= 1 = sp, 2 = sp2, 3 = sp3 01- sp2,…

A: Given  Structure is given  Hybridization of given centre = ?

Q: la How would you accomplish the following conversion? A) H+/H20; HCN B) -OH/NaCN C) Br2/H+, H20;…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: 2. Calculate [H*] and [OH] for the following : [H* [OH a) pH = 3.0 b) РОН %3D 2.60 с) РОН %3D 5.63…

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Q: Draw the products of the reaction shown below. Use wedge and dash bonds to indicate stereochemistry.…

A: Given reaction:-

Q: I H₂CO H III Н С H₂CO H.C Н Identify which of the following compounds is meso. OCHII H₂CO CH3 H₂C H…

A:

Q: H3C-CH₂-CH₂-C-OH CH,CH,NH, hoot H₂O +

A:

Q: 13. Complete each of these following reactions (i.e. fill in the boxes with the missing reagent(s)…

A: Requirement from question: Incomplete reactions given. Need to write required reagents in boxes.…

Q: Identify the meso compound or compounds. H. H. H. Br-C-CI Cl -C-Br Br -C-CI C-Br Br-C-CI Br-C-CI…

A: Meso compounds are the compounds are optically inactive in nature. Meso compounds are achiral…

Q: Choose correct reagent(s) for the conversion below al propanoyl chloride with (1) AlCl3 and (2) H₂0…

A: Friedel-craft alkylation: Benzene reacts with alkyl halide in the presence of Lewis acid to do…

Q: 6. What is the principal product of the reaction shown? 0— CH2CH3 + I-CH₂CH3 a. OH + HOCH₂CH3 b.…

A:

Q: H H H H H H Lower Energy H H OH Br Compound A-1 OH H Compound A-2 CI Br H Br Compound C-2 CI H H H…

A: Given are Newman projections for organic compounds.The most stable i.e. lower energy conformation is…

Q: For each of the pairs given, predict which acid is stronger ) H2Se and H2Te ) HCIO2 and HCIO3 ii)…

A: i) H2Se and H2Te The given acids are diprotic acids. The size of Se is smaller than Te, as atomic…

Q: Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the…

A: Alkene gives an electrophilic addition reaction with hydrogen halide to form an alkyl halide. The…

Q: H₂N A) KI ITS O B) i) NaNO2, HCl ii) KI C) i) NaNO₂ HCl, ii) 12 D) 1₂

A:

Q: Practice : Name? (а) H CH3 (b) H I-Cl - Cl H3C' `H. H e2004 Thomson - Brooks/Cole (а) H (b) H3C…

A: We need to tell the IUPAC name . Since you have posted question with multiple subparts. As per…

Q: (Practice Problems) H. CI 1) CH, - OH H,C CH, H,C - H,C Cн, - Br 6) OH 2) CH - (CH3)2 H,C H. H;C. 3)…

A:

Q: None

A: Given:To get the heat of reaction, we first identify the bonds broken and formed.Base the values of…

Q: The following compound is? O a. sz O b. none of the other answers O c. R,S O d. S,S O e. Z,Z O f.…

A: The molecule is chiral, so we assigned the absolute configuration to the allene. In naming allenes,…

Q: a) OH Reagent(s) for a: но.. OH

A:

Q: PLEASE DRAW OUT PRODUCT H2 Uz, 1 1. HONO 2. 2.CUBr Raney Ni NO2

A: 1,3,5,7-Cyclooctatetraene (COT) is an unsaturated derivative of cyclooctane, with the formula C8H8.…

Q: Phenol Water Phenol mole %phenol ar) T °C mol mol fraction gr gr 10 4 35 10 46 10 6 50 10 8 58 10 12…

A: Topic -- Finding the value  1. Moles of phenol 2. Moles of water 3. Mole fraction of phenol…

Q: 5 cobalt (III) sulfide 6 7 sodium phosphide 8 iron (III) iodide 9 strontium chloride nickel (II)…

A: Answer:- This question is answered by using the simple concept of writing the chemical formula for…

Q: ich of the following compounds have a mirror plane? f a e d

A: We have to tell which option are correct

Q: c) d) e) f) H.C -CH3 -CH3 NaCN ОН 1) BrMg CH OH H₂SO4 CH3 2) HạO* H OCH OCH _NH2OCH3 CH3 CN CH 3 -он…

A:

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.