1. 1eq. Eto /E£OH OEt 2. H30® Dieckman cyclization product ОН Anhydride NH2 1ед. 1eq NaOH O=

Q: Determine the product of the reaction: CH,—сн—CH,—он + н ČH, a) CH,-CH-CH, Cl b) CH3-CH-CH3 CH3 c)…

A: In the given reaction, the reacting species is 2-methyl-1-propanol. It is primary alcohol that…

Q: Determine the product of the ff. rxn steps 1. CH;NO,/OH- 2. Sn/HCI 3. ΗΝΟ A. В. C. D. OH -NO2 NH2 OH…

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Q: (c) OH (d) Br ? ? Eight or fewer carbons Acyclic compounds OH Br

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Q: D (C3H1204) H30* heat heat E

A: A scheme is given to us . In this scheme we have to identify unknowns

Q: Determine the product in the following reaction (ignoring possible stereoisomers). CH3SH H 'Br

A: Observing the given reaction, it is clear that the CH3SH is a weak nucleophile. So first being the…

Q: 1)) Determine the structure of the products in the three reactions and indicate if the final product…

A: HNO3 - H2SO4 is a nitrating mixture that undergoes nitration in benzene.  KMnO4 is an oxidizing…

Q: R*R?CHOH-CR®R* R'R?C=CR®R* uld orientation of each substituent in reactant to convert it into…

A: solution- reaction -  R1R2CHOH -CR3R4   →   R1R2C=CR3R4 assuming, R > R2, R3 >R4R1  and R2 we…

Q: Draw the product or products of the reaction. Include charges where appropriate. Draw the…

A: When acid react with base form salt.

Q: X= muclaophile 3. C-C-2-e + ビメ → + HX > what in the diterence? 00 ニ- 2HaC 0ー ーとーロH +N-Cビ-0H →…

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Q: AICI3 Zn(Hg) HCI para product L Toluene Succinic anhydride SOCI2 H2SO4 NABH4 AICI3 N M heat P.

A: Series of reaction: In the series of reaction, when the reactant 'X' converted into product 'Y'…

Q: rxn 1.png R2'NH A + R OR R NR2 (A) (В) A) Addition B Elimination c Substitution D Rearrangement

A: It is nucleophilic acyl substitution reaction which proceeds through addition - elimination…

Q: II. Multistep Synthesis. Supply the missing compounds/reagents. H,C HBr FeBr BH, EtO HC H,C но. Br.

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Q: Which involve .7 .interconversion reaction A. Rearrangement reaction. O B. Elimination reaction. O…

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Q: In an associative substitution reaction а. AS# > 0 b. AS# 0

A: Entropy is the measure of randomness or molecular disorder in a system. It is numerically equal to…

Q: leianments Write All products indicate possible and major and minor where appl CH-CHs neat CHoll…

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Q: 409). (D149) OH H. OH coo -N R374 но. OR 1st Step (E117) ROH (Y409). (D149) OH OH R' -N R374 но-…

A: Acids: The organic compounds which have the tendency to donate H+ ions(protons) For example HCI…

Q: h) ? (name, str, stereochem) -----cold dilute KMNO4---- (±) erythro pentane 2,3 diol H- HHOH CHCH i)…

A: h) cis compund + cis addition results  erythro pentane-2,3-diol. i)  3E -hex-3-ene reaction with…

Q: Cuando se añade H-Br a un alqueno terminal el producto sigue la regla de Markovnikov. O a. Cierto O…

A: Note: According to our guidelines we are supposed to answer only one question.  Kindly repost other…

Q: OBYJU'S Step -1 „OH +K - 12 H, - KBr

A: Organic chemistry is branch of chemistry in which organic reactant react to form organic products.

Q: R'R?CHOH-CR*R* R'R?C=CR°R* t should orientation of each substituent in reactant to convert it into…

A:

Q: e) 9-bromo 5-methyl 2-nonene -----H2, Ni 900°C---------- ? (name, str, stereochem) Cl2, CH2C12 f)…

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

Q: R'R°CHOH-CR'R* R'R?C=CR*R* What should orientation of each substituent in reactant to convert it…

A: The given reactant is alcohol. The reaction given above is a dehydrating reaction. Here the alcohols…

Q: 59. Rate of Substitution Reaction I. S. S. Br Br

A: We have given the substitution reaction and we have to find the rate comparison between the two…

Q: Reaction Of ALIPHATIC AL COHOL conc H2SO4 CH;COOH conc H2SO4 + reflux CH3 Na CH;ĊCH,CH3 OH + PCI5…

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Q: PCk H,-Pd BaSO4 CH;NO, 1,0 CH;O OCOC- CH;0 CO,H СНО NAOH (Rosenmund reduction) OCH3 OCH3 OCH3 OCH3…

A: PCl5 is a chlorinating agent. In Rosenmund reduction acyl chloride is reduced to an aldehyde.…

Q: 1. H3C. CH3 ? ? + 1,2-Product 1,4-Product HBr (1 eq) 2. + Br2 ? ? (1 eq) 12-Product 1,4-Product 3. ?…

A: All these are examples of conjugated dienes which are more stable than simple or isolated dienes…

Q: KHS2O3 + H2O --> (?)

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Q: HO (i) (R)-2-bromobutane 25 C 25"C ) ()-3-Bromo-3-methylhexane MeOH (k) (5)-2-Bromooctane MeOH, 60°C

A: SN2 Nucleophilic substitution via second order Strong nucleophile+ good leaving group+ primary or…

Q: Complete these SN2 reactions, showing the configuration of each product.

A: SN2 reaction or bimolecular nucleophilic substitution has following features: Formation of a…

Q: What is the product of this reaction sequence? Br Otrans-5-methylhex-2-ene O trans-2-methylhex-3-ene…

A: Since, you have multiple question. So, I will solved first question for you.  You can see the…

Q: 1. Sort the following molecules into the quadrant in the chart shown below that best describes them.…

A: The basic concept of the base is it gives hydroxide ions when ionized completely. A strong base is…

Q: C2H4 + CH3CH2LI produce: O C2H4+Li+ CH3CH3 O CHCLI + CH3CH3 O C3H6 + H2 O C3H5LI

A: Given reaction is : C2H4+CH3CH2Li→?

Q: 2n-BuLi ThE 30 c° NHCOZ-Buc 2+-1B4 me thent mel-70 54% CHO 79% 5-azaindole whate the Mechanits is

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Q: Which halide is most reactive in SNl reactions? Select one: CI CI H3C CI CH3 CH2CI CI

A: The SN1 reaction is a nucleophilic substitution reaction. It is a two-step reaction where the first…

Q: h. SN1 SN2 E1 E2 CH3H OH + SOCI2 Product(s)/Stereochemistry(ies) of reaction h

A: The products are given below -

Q: H H.. \PPH3 Rh: insertion A Ph;P" CI H2C=CH2 CO PPH3 -PPH3 Ph3P-Ru 'PPH3 čo +2 Ph-CEC-Ph B.…

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Q: Draw the products of attached reaction, including stereoisomers.

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Q: CH3 o-nitrotoluene CH3 NH, CI 2 o-toluidine NO2 NH,HCO2 10% Pd/C Step 1 1) NaOAc, H₂O 2) CI Step 2…

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Q: Draw stepwise mechanisms illustrating how each product is formed.

A: The stepwise mechanism for the given reaction can be illustrated as follows,

Q: MeO2C Li -N(allyl)2 MeO NH3 - ELOH Br Pd(PPH3)4, Cul

A: 1st One is birch reduction. -OMe is a electron donating group. Benzene ring reduced with 2 double…

Q: 1. HgSO4 H20 Cl2 2. NABH4 how stereochemistry

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: Match each alkene to its heat of hydrogenation. Alkenes: 3-methylbut-1-ene, 2-methylbut-1-ene,…

A: The structures of given compound are shown below:

Q: What is the product of the following reaction? H3C-CH,-CH=CH2 HBr JF-MO5 H;C-CH-CH2-CH3 Br JF-MO5а…

A: Anti Markovnikov rule portrays the regiochemistry in which the substituent is clung to a less subbed…

Q: i. 4-ethoxy-2-methyl-hex-1-ene j. 3-isopropoxy-butan-1-ol

A: Given,  i) 4-ethoxy-2-methyl-hex-1-ene  j) 3-isopropoxy-butan-1-ol

Q: Rank the following from most reactive to least reactive in an E2 reaction

A: In E2 reaction, anti-elimination is always favoured over syn-elimination because staggered…

Q: 16) SN1 S-2-bromohexane C,H;OH +

A: In SN1 reaction two isomeric products are formed.  In first step formation of carbocation takes…

Q: C HCI ÇI NaOH F G H A DMSO (Transition State) (Product) Br,(aq) CH,CH,ONa Δ B (Level 2 only) D…

A: DMSO or Dimethyl sulfoxide is a polar aprotic solvent which does not have any hydrogen bond with the…

Q: Me Me OMe OMe OH & OH OMe COMe BF 3'OEt2 Mgl2 A B show relative stereochemistry show relative…

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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.