Write down a mechanism for this reaction: Br Br

Q: NH2 H* -H,0

A: Ketone when react with primary amine forms imine as a product.

Q: CH3OH ? Br

A: The given reaction is unimolecular nucleophilic substitution reaction (SN1). In this reaction…

Q: 1. (4) Complete the reaction and show the mechanism Br (CH3)NΗ (xs)

A: The given reaction follow SN2 mechanism.  The product formed is shown below:

Q: When analyzing the starting materials and the products that follow from the following reaction, what…

A: The reaction of the starting material which is a haloalkane undergoes dehydrohalogenation and forms…

Q: 2. What Alkene would be used to synthesize 3-bromohexane? + HBr CH;CH,CHCH,CH,CH; br 3. Write down…

A: Reaction proceed through the most stable carbocation. It will give the major product . Carbocation…

Q: :ce Consider the following reaction. MgBr HCI Et20 H20 a) What is the structure of product A and…

A: The detailed solution of the reaction are provided in attach image.

Q: OH 1. CH3-MgBr CH3 Еxcese CH3 2. H20 CH3OH

A: Please find your solution below : Since you have asked multiple question, we will solve the first…

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

A:

Q: HN. HO:

A:

Q: C = C1H CH3 2 NaNHa 31 H+ 000

A: See mechanism below.

Q: 4. (a) Complete the following reactions and provide mechanism of the reactions involved. -CO2Et CN…

A:

Q: Please explain/show the mechanism for this reaction

A: The given reaction is

Q: Write the expected substitution product(s) for each reaction and predict the mechanism by which each…

A: The given alkyl halide is an example of secondary alkyl halide since the bromide is attached to a…

Q: 1' CH,ONa H,C CH 2 HO CH3

A: The given reaction can be carried out by Robinson annulation.

Q: -CO2H OH

A: This is hydrolysis of acetal linkage and after that this is esterification reaction

Q: Propose a mechanism for the free-radical chlorination of ethane,CH3¬CH3 + Cl2 ¡hv CH3¬CH2Cl + HCl

A: In presence of light Chlorine molecule shows homolytic fission to give free radicals   this step…

Q: H2O ? .CI Br2/H2O ?

A: Water is a polar protic solvent and the alkyl halide is tertiary which favours Substitution…

Q: Explain the mechanism and reactions that occur in the schematic below! 1) Dimethylcarbonate NaH, THF…

A:

Q: Identify the products X and Y in the following reactions and propose suitable mechanism for their…

A: ->SeO2  is oxidizing agent and give alpha oxidation.

Q: Discuss the mechanism and desirable products of following reactions: Br * acetone OH

A: When alkyl halide is treated with alcohol, both substitution and elimination reaction is possible…

Q: What is the mechanism of this reaction? Please include details about the steps. Thank you...

A: In the first step of the given reaction, Br- (leaving group) gets eliminated forming a secondary…

Q: What is the most likely first step of this reaction's mechanism? CH3 CH;CH2OH Br

A: The reaction given is SN2 reaction in which the nucleophile attacks and removes the leaving group.…

Q: d. 2 ea Brz e. 1 eq cl2 f.

A:

Q: How many acid-base steps occur in this mechanism? :OH :OH ₂ H CI: -H₂O (C5H₁2O) (C5H130+) (CgH*)…

A: Acid : Proton donar. HCl is acid because it will provide protons. Base : Proton acceptor. Here…

Q: CH3 HI H3C-C-OH CH3

A:

Q: Br H20

A:

Q: 1. Outline mechanisms for the following addition reactions. (a) HBr (b) ICI (c) HI

A:

Q: Br CH3OH 250с

A:

Q: Propose the mechanism for the reaction below and use resonance structure to explain why the other…

A: Hydrobromination of alpha beta unsaturated ether

Q: 101 + 1 MeO Na MeO 100

A: The given reaction is a polymerisation reaction.

Q: 2. Provide the mechanism for the reaction illustrated below. Show the relevant…

A: Given reaction: We have to write the mechanism of this reaction.

Q: Rank these alkyl halides by their SN 2 reaction rate. Br CI Br Br A D

A: SN2 Reactions occured in single step, leaving Nucleophile and attacking of Nucleophile takesplace…

Q: NaH + H; + EO OH

A: NaH acts as strong  base and and form hydride ion, H- . It abstract hydrogen from alcoholic group.…

Q: Br Pd°Ln Me Me MeCN, EtzN Me Me

A:

Q: Draw a structural formula for the major organic product of each reaction and specify the most likely…

A: SOLUTION: Step 1: The above given reaction is the reaction of allyl chloride with sodium ethoxide.…

Q: HBr Br HO 65°C

A: Protonation of alcoholic oxygen  Loss of water molecule as a leaving group  Carbocation…

Q: H20 Br2/H20 b)

A: Alkyl halide gives solvolysis reaction water. The reaction completes in two steps. In the first…

Q: HBr Br LOH 65°C

A: In the given reaction the alcohol reacts with hydrogen bromide to form alkyl bromide. The reaction…

Q: 5. Propose a reaction mechanism for this reaction. COH (1) NaH PPh3Br

A:

Q: cEN OH OH `NH2 + NH3 H20 H20

A: Butyronotrile is a cyanide with the formula C4H7N .This is a colourless liquid miscible with most…

Q: HNO3 H,SO,

A: Given a chemical reaction and we are asked  the name of the mechanism for this reaction.

Q: 1) МezNH 2) НСНО, H* 3) CH3I 4) Он-

A: The reaction is the shift base formation.

Q: H3C, "OH CEN

A:

Q: 1. Write the major organic product and the complete reaction mechanism (for a and b only) shown…

A: The reactions given are,

Q: What is the mechanism for this reaction?

A: The addition of halogen molecule across the double bond of unsaturated hydrocarbons is termed as a…

Q: S 1. 2. H3O+ FO, AICI 3

A:

Q: Br -OK ELOH 3.

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

Q: 9. a) Draw the structure of the product of this reaction. b) Write out all the steps in the…

A:

Aldehydes and Ketones

Aldehydes and ketones are organic compounds that have a carbonyl group, C = O, as their functional group. They both differ in the placement of this carbonyl group in their structures.