4. Provide a arrow pushing mechanism for the following transformation. H3O+ Br2

Q: 2 Show all steps in the synthesis of GVA using the tert-butyloxycarbonyl (Boc) group as a protecting…

A:

Q: Classify following solvent as protic or aprotic                 CH3NO2

A: Protic solvents are those which contain protons bonded with high electronegative atoms like oxygen…

Q: Show the complete arrow-pushing mechanism for the following transformation.

A: The complete arrow-pushing mechanism for the following transformation can be shown below

Q: Question 12 of 30 > 0/1 Propose an efficient synthesis for the following transformation: The…

A:

Q: Design a two step synthesis that converts 3-pentanone into 3'-pentyl acetate as shown below. H2 -CH3…

A: we can convert  one functional group to  another by various reaction pathway like substitution or…

Q: OMe HO 1. LIN(iso-propyl)2 OMe 2. H20

A:

Q: Based on the image attached, explain the step-by-step mechanism reaction of reduction for…

A: LAH  Lithium alumnium hydride is strong reducing agent It reduce ester into primary alcohols  via…

Q: 3. Please provide a complete step-wise synthesis of the target molecule showing all steps, reagents…

A: Benzene on F.C.Alkylation to form Methyl benzene (Toluene) in first step. Then Toluene undergoes…

Q: DMSO 0

A:

Q: Classify following solvent as protic or aprotic                CH2Cl2

A: Protic solvents are solvents which contains protons bonded with high electronegative oxygen and…

Q: Perform a retrosynthetic analysis and suggest a synthesis of the target molecule (on the left) from…

A: The Retrosynthesis method is the method that determines the starting material by the fragmentation…

Q: From the list below, select all of the benzene derivatives with activating groups attached. CHO…

A: Activating groups on benzene increases electron density of benzene via +M effect whereas…

Q: If a large excess of the nitrating reagent is added, does the product produced contain one nitro…

A: Given: Excess of Nitrating mixture To find: Product will have one nitro group or more than one nitro…

Q: Write a detailed, stepwise mechanism for the following reaction. CH3 Cl2 -CH2CI + HC1

A: The structure in which the electrons are delocalized on the three or more atoms which cannot be…

Q: ore Br

A:

Q: NaBr Acetone NACN DMSO NC NC EtzN: DMSO

A:

Q: Explain the features of E1 reactions are worthy of note ?

A: Elimination reaction is a type of reaction is mainly used to transform saturated compounds (organic…

Q: Show the arrow pushing mechanism for getting tropylium ion from the benzylic carbocation

A: In the given question we have to rearrange the benzylic carbocation to tropylium ion.

Q: Draw the structure of 3-bromo-5-methoxybenzoic acid in the window below.

A: Given : IUPAC name of molecule.  Step 1: draw benzene structure Step 2 : add cooh group to any…

Q: Br-

A: Note: Olefin undergoes electrophlic addition reaction. But the cyclobromonium ion is opened by…

Q: OCH3 NH, OCH3

A:

Q: Show the relationship between E2 Reactions and Alkyne Synthesis ?

A: Interpretation: The relationship between E2 reactions and alkyne synthesis is to be shown.

Q: 2-methylbutanoyl chloride

A: Organic reaction mechanisms

Q: 0. FeCl3, Cl₂ 0 Cl

A: Anisole undergo electrophilic substitution reaction when reacted with Cl2 and FeCL3 to form O-chloro…

Q: Show Dehydration Using POCl3 + Pyridine—An E2 Mechanism ?

A: Dehydration of alcohols with the help of phosphorus oxychloride POCl3 and pyridine (a base of amine)…

Q: What organic product is formed in the following reaction? (Note: here an ethyl group is not a…

A:

Q: he Table of Reagents, select those that would be used to carry out the following transformation: NH2…

A: A sequential reaction is given and asked what appropriate reagents are used for this reaction.

Q: 2. Write a synthesis of the Wittig reagent C1

A:

Q: 2. Propose a complete and accurate arrow pushing mechanism for the reaction below. HNO3 H2SO4 O2N 3.…

A: Nitration: It is the chemical reaction in which there will be the addition of nitro group (NO2) to…

Q: (i) D CD3 (i) (ii)

A: The reaction taking place is given as,

Q: For each equation state the major reaction pathway that it will undergo. O Hold and drag to reorder…

A: The type of reaction to form major product can be determined by the reaction conditions.

Q: Provide the reagent that is needed to perform the transformation shown below. (Use the Reagent…

A: Reagent:-Reagent is a substance or mixture for use in chemical analysis or other reactions.

Q: .From the two synthetic routes shown below which one would be the best route for the desired…

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Show the difference between SN1 and E1 Reactions ?

A:

Q: From the two synthetic routes shown below which one would be the best route for the desired product.…

A: 1) the reaction of cyclohexane react with NaBH4 to give cyclohexanol. because the NaBH4 is reducing…

Q: 7.33 3-Hexyne을 어떻게 propanal로 변환할 것인가를 나타내어라. 과녁 분자의 모든 탄소 원자들 은 가능한 한 출발 물질로부터 공급되어야 한다. 합성 과정에서…

A:

Q: -CH, CH, HyC

A:

Q: Step 1 1. LIAIHG i H30* guench ÇO̟Me CO,Me Compound 1 2. PCC Step 3 Step 4 Step2

A:

Q: 1. Compound2 may have an electrophilicreaction because of its saturation 2. Compound1 must undergo…

A: Since double bonded and triple bonded compounds are in unsaturation condition whereas single-bonded…

Q: Propose an explanation for the fact that the trifluoromethyl group is almost exclusively meta…

A:

Q: 2. Draw out the forward synthesis (fill in the boxes) only for the following transformation (it'll…

A: Here we have to make a desired forward synthesis for below conversion .

Q: Predict the product of this E2 elimination reaction. 1 ||| Br H3C Ph f Ph Ph H3C Ph Ph H CH3 Ph ||…

A: In case of elimination reaction , anti position of H and leaving group gets favourable . In this E2…

Q: Show an actual arrow-pushing mechanism for the transformation below, and briefly explain the…

A:

Q: Provide a detailed arrow pushing mechanism for the following transesterification reaction. H* +…

A:

Q: CH3 CH3 Br FeBr3. HBr (а) Br2 ČH3 CH3

A:

Q: 5. Provide a complete curved arrow mechanism for the most straightforward conversion of 5 and 6 to…

A:

Q: A set of three nucleophilic displacement reactions is shown below: CH3 SOH CH3CH2ĊCH3 SN1 reaction

A: GIVEN

Q: For the following reaction, provide an arrow-pushing mechanism and the product. Ph₂P. KOtBu e Br

A:

Q: CH3 НО KMNO4 OH- H* TOULENE BENZOIC ACID

A:

Amines

Amines are organic compounds with a nitrogen atom having a lone pair of electrons on it. They are derived from ammonia (NH3) wherein hydrogen atoms are substituted by an aryl or alkyl group.