HCO2ET, NaOMe ? RT, 30 min 94 % H.

Q: Br2. UV Cう Ciz. ーH

A: Alkane in presence of UV light and Cl2 or Br2 undergoes free radical chlorination/bromination.  in…

Q: H* OMe., |OMe

A:

Q: CI I) KCN 1) HBr = 11) C12 OK Br CI

A:

Q: plete the following reactions ( . H2SO3 + Ba(OH)2 > . CAH9OH + 02 > Br2 + YF3 >

A: In the balanced chemical reaction number of atoms of each element in product side is equal to number…

Q: 5. Give the mechanism and product for the reaction below. CH,OH "CH,CH,

A:

Q: The following initial rate data are for the reaction of tertiary butyl bromide with hydroxide ion at…

A:

Q: LIAIH4 H20

A: Lithium aluminium hydride is a very good reducing agent used in the reduction of aldehydes, ketones,…

Q: :0: а.) H3C 0-H H3C :0: :0: H b.) H-C-Br: CH3 :Br: H3C H3C c.) +

A: We know that, Polar molecules are those which have charge separation between them. Non-polar…

Q: OMe OHC, KOH/ N OMe ÓMe OMe OMe ÓMe

A: Nucleophilic addition reaction: Addition reaction in which an nucleophile is added to electrophilic…

Q: Q. 4. Complete the following reactions and indicate the steps involved. CH3 CH3 Silica gel CH3 H,SO,…

A:

Q: LOH HO Toluene, A 5-10 min °CO2H

A: This reaction is basically [4+2]-cycloaddition reaction occurs in presence of heat.

Q: Indicate the scheme and detailed reaction mechanism of the reactions: ZNCI, a) СҢ СH, СH,CH, ОН +…

A: Primary, secondary and tertiary alcohols are distinguished by using Lucas reagent (Anhydrous ZnCl2…

Q: H,O, H,SO,(cat)

A: The key product of this reaction is a ketone formed by tautomerization and this reaction proceeds…

Q: HOH2C HOH2C, HO но- но Но OH OH ´OR Br Show the synthesis of the molecule below, please show the…

A: The organic reactions are carried out with a specific mechanism under the guidance of reagents.

Q: d) what is tre full maartion mechanism Of Entry #4 reaction. e) Adraias unat is tre trend observed…

A:

Q: Suggest a plausible mechanism for the reaction shown below Mo Ie OC -Mo OC Br Hint: The first step…

A:

Q: 1) H2O2 (iii) 2) PC13 3) H2O ČOOH

A:

Q: H,SO4 HO.

A: Given reaction is;

Q: 0. el

A: Applying concept of addition elimination reaction.

Q: Hg(OAc)2 H,O/H,O*

A: This reaction is a oxymercuration reaction.

Q: CF3 .CF3 Meo

A: The ether is generated from the reduction ester in the sight of the LiAlH4 / BF3 and Et2O.

Q: In your own words, please describe the following reaction mechanism in detail, and also describe any…

A:

Q: 67- g/ Give a reaction mechanism OH EtO,CN=NCO,Et ʼNO2 CH2NO2 PPH3 92%

A: This reaction is  Mistonbou inversion reaction where inversion of a nucleophilic centre takes place…

Q: HO H. H. NH OH HNO3 N. H,SO, HO HNO3 N. CH3 H,SO4

A: "Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: 1) Base 2) H2O CHO NO2 80%

A: Nef Reaction: Reaction involving the conversion of nitro compound into carbonyl compound.

Q: Give the organic chemical reaction mechanism of the synthesis of 1-bromobutane. link of the video…

A: Given Give the organic chemical reaction mechanism of the synthesis of 1-bromobutane.

Q: Predict a possible mechanism: a. 1. MgBr 2. H,0 b. 1. LAH "NH2 2. H20 c. Ph;P-CHCH,CH,CH3

A: Dear student , I am authorized to answer only first three subparts of your question as per…

Q: 2. Complete the following reactions and provide the reaction mechanism: Br2, FeBr3 H*

A: The hydrogen atom which is present in the aromatic ring is replaced by the electrophile is known as…

Q: .CO,Et LIAIH4 ОН Zn. HBr Me Me Me ACOH, H20 RT to Reflux, 50 min, 63% Et20 Reflux, 3 h, 100% Write…

A: The mechanism of the above reaction is given below -

Q: raw step 2 of the mechanism. + H,C TV Ź + I +t + +1

A:

Q: (d) Br CH₂OH ? (e) CI NaBr DMSO ?

A: (d) The given starting compound has tertiary carbocation on dehalogenation (removal of Br) thus it…

Q: HO 1. NaH 2. CH,CH,Br 1. CH,CH,OH/ (CF,CO,),Hg 2. NaBH,

A:

Q: Complete the mechanism for the reaction of 2-butanol in sulfuric acid at 140 °C by adding any…

A: The given mechanism for the reaction of 2-butanol in sulfuric acid at 140 °C is to be completed  by…

Q: C,H140 (d, 3H) (d, 3H) (d, 3H) ан, 3 lines) (IH, 5 lines) (5 peaks, 1H) (O-H) (5 peaks, 1H) PPM 1-…

A: Nuclear magnetic resonance is a technique that is used to predict the structural formula of the…

Q: Q2. Show the mechanism of the following reactions. N3 THF, rt `Br + NaNg reflux i. + CH;OH a ii.…

A: i) Axial attack of N3- is favored  ii) The reaction undergo SN1 mechanism. iii) The reaction…

Q: с-НCI (1 drop) H. OCH2CH3 H2N NH2 O2N ethanol, reflux 1. major product 2. the most plausible…

A:

Q: Hi/hegt HO.

A:

Q: 2. Predict which reactions proceeded by an SN1, Sn2, El or E2 mechanism: Br NaOCH,CHa OCH CH3 + NaBr…

A: Answer: These reactions can be characterized on the basis of type of reactant and solvent that is…

Q: 8.50 The initial rates for the following elimination reaction were measured under different…

A: The rate of reaction expresses the change in concentration of reactants or products at a particular…

Q: 2 a и H Na₂Cr₂0 21₂0, NHS Cl₂cla, Acetone 10% pd/c, Ammarium formate Eto Ac Meok=1:1 E

A:

Q: Suggest a reasonable mechanism for the reaction shown Br here. HO CH;CH,OH

A: The given reaction is shown below:

Q: Q2/ Write a suitable mechanism in full details for the following reactions. ReHa NH3 R-ER NH 1- 1.…

A: benzene are reactive in nature and they generally undergo electrophilic aromatic substitution…

Q: 30. The rate of zero order reaction (y-axis) against the concentration of the reactant 31. The…

A: Chemical kinetics is the study of the reaction that how fast or slow a reaction is taking place. The…

Q: D. Provide a reasonable mechanism for the following reaction. ·CCL 3 1. NaOH, H₂O 2.H₂O* он

A:

Q: Br 1) NACN, DMSO 2) excess LAH 3) H20

A: Organic reaction mechanisms:

Q: In the reactions below, there is a main reaction step followed by one or more workup steps (which…

A: Work up stage is very important For organic synthesis . This is the purification stage or to remove…

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.