anks with either "syn" or "anti". hemistry found in the product of an electrophilic addition to an alkene is related to the mechanism of the reaction. Usually as additions result from both new groups adding in a single concerte additions result from a 2-step addtion.

Q: Please drauuthe Mechanism for+this polumentzoben

A: Chain initiation step include,

Q: Draw the products of attached reaction.

A: The products of attached reaction can be shown below, Epoxide ring opening reaction:

Q: What is the reaction mechanism for

A: gyi

Q: Enol form in the mechanism of * halogenation is present.step Fast Slow Both

A: Answer :- Enol form in the meachnism of halogenation is present fast step.

Q: The regiochemistry in the electrophilic addition reaction shown here does not adhere to the original…

A: Markovnikov's rule  : This rule is applicable in electrophilic addition in C=C double bond.…

Q: what is the rate of reaction for the attached reaction?

A: Since it is not given whether the reaction is elementary or complex. Hence I'm assuming it to be…

Q: please show the Correct mechanisms, and how do you decide which product is the major or minor???

A: Please find the attachment

Q: Classify the type of elementary step based on the mechanistic arrow(s) shown below.   A) homolytic…

A: If the bonding electrons are evenly distributed among the bonded aroms are called homolytic…

Q: Complete a mechanism for the given reaction.

A: In the above reaction, we have reactant 2 with carboxylic acid and alcohol functional group. Hence…

Q: Halogenation using the mixed halogen ICl can feasibly lead to two different products, as shown here.…

A:

Q: The initiation step in a free-radical halogenation involves mechanism. OA. homolytic, one OB.…

A:

Q: The requirement for inher sphere mechanism is that one of the reactants is low spin non labile, the…

A: Requirements of inner-sphere mechanism- 1) one of the complex or central metal atoms must be low…

Q: Please draw arrow-pushing reaction mechanism and identify number of electrons involved here. This is…

A:

Q: PHNHNH,, HA NABH,, CH,OH LOH O: HO H,SO, (cat.)

A: Mechanism for all the reactions is given as follows:

Q: Which mechanism is incorrect? They all seem correct as the halides are attached to the secondary…

A: No answer is not E  The correct answer is D .

Q: Consider the pair of reactions. Draw the organic products, then predict the type of substitution…

A: Answer: Reaction (1) and (2) both are SN2 mechanism Explanation: 1)Since in both the cases substrate…

Q: Which is faster, why? # of products for each reaction? What is the mechanism of each reaction?

A: Given reaction is William son synthesis reaction in which nucleophile attacks on the alkyl…

Q: Synthetic

A:

Q: Complete the following reaction scheme , Complete the following reaction scheme

A:

Q: Show the COMPLETE mechanism of the reaction.

A:

Q: Why energy required to reach transition state is lower in active site? And not Lowe in any other…

A: In a particular reaction, the minimum amount of kinetic energy required by the reactant molecule to…

Q: Is the given mechanism is correct or not,please confirm?

A: Yes, the above reaction to acid catalyzed ring opening of epoxide. So, the first step is attack of…

Q: Please show mechanism and explain every strep

A: We have to predict the mechanism for given reaction

Q: Perform the following reaction mechanism:

A:

Q: Draw curved arrows to depict the third step of given mechanism. H.

A: Since there are lone pair electrons on the O of water. Hence it will take the proton from the…

Q: mechanism

A: Starting material React with ethanol in acidic medium formed ester Product.

Q: Which can ot be used in the second step of the reaction sequence

A: Azide ion is a strong nucleophile (far better than amines) and will readily participate in…

Q: Consider the mechanistic step shown below. Which of the four characteristic patterns of arrow…

A: We have to predict:  Arrow pushing pattern  Place for Head of curve arrow.

Q: Brz. FeBr NaOMe

A: Organic Transformation and Mechanism

Q: Initiation step for (ethane and chlorine)

A: When ethene is treated with Chlorine Molecule, then it follows free radical mechanism, in which…

Q: Draw the products of attached reaction by following the curved arrows.

A: The product of attached reaction is determined as shown below,

Q: Show the complete mechanism. OTs A or H3C, OTs В

A: The given compound gives a solvolysis reaction in ethanol solvent. The reaction completes in two…

Q: For the following reaction, draw a complete reaction mechanism using curvy arrows being sure to show…

A: Solution Two sensible sources of binary compound-like reactivity ar the complicated metal hydrides…

Q: major ProdvCtS on only -ome H3PM, anes Et, NH

A: in organic chemistry functional group can be converted to another functional group via certain…

Q: This is a hydrogenation and carbene addition problem. How do I find what the missing reactant is of…

A: Interpretation: We have to tell the reactant for the following reaction.

Q: ОН SAM Products ???? Mechanism????

A:

Q: Can you draw the mechanism specifically for the cleavage part,

A:

Q: For the photochemical halogenation reaction below, draw both propagation steps and include the…

A: photochemical reaction Photochemical reactions proceeds through   free radical mechanism Tertiary…

Q: Add any remaining curved arrow(s) to draw step 1 of the other possible mechanism. Modify the given…

A:

Q: What is the complete mechanism for this F!she rxn?

A: When carboxylic acid is treated with alcohol in the presence of mineral acid, generally H2SO4, we…

Q: Choose a functional group from the molecule. Draw a reaction mechanism showing this functional group…

A: The arrow and mechanism given below.

Q: rmed for a split second before breaking into the products

A: When molecules of reactant cross the activation energy Barrier then these molecules form transition…

Q: For each of the series of electron-pushing arrows, please draw the respective products. Also,…

A: Since, you have asking to solved the multiple subparts questions, so I will solved first three…

Q: Rank the following substrates in order from slowest Sy2 reaction rate to fastest. Br H3C Drag answer…

A:

Q: Use mechanism to explain the products of this reaction. Which product would be the most abundant?…

A: The mechanism of the given reaction is : Step 1 : Under UV light, Br2 undergoes homolytic cleavage…

Q: Draw ONLY curved arrows for each step of the following mechanism:

A: Carbonyl compound gives nucleophilic addition reaction due to electrophilic carbon atom. Carbonyl…

Q: of elementary step based on the mechanistic

A: It is Tertiary Alkyl halide. So, it follows Sn1 mechanism. And it is two step mechanism.

Q: Draw the products of attached reaction by following the curved arrows.

A: The products of attached reaction by given the curved arrows can be drawn as

Q: Hello, I am very confused working on this worksheet, please help me understand every step for either…

A:

Q: excess

A:

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.