() HCI BH, THE HO2 OH (6) Br H,0 (v) 1 b. Device a stepwise mechanism to obtain the below product. Mention curved arrow and most stable carbocation formation (CO3, H,0 OH

Q: What alkane is needed to make each attached alkyl halide by radicalhalogenation?

A: The given alkyl halides are represented as follows:

Q: The best reagents to carry out the reaction at right would be: a. O c. CH₂ Hg(OAc), H₂O NaBH4 KOII…

A: The given reaction is :  What is the best reagent to carry out this reaction towards right side ?…

Q: Hg2+ Но c=CH2 H3C H3C-C=C-H H30

A:

Q: Write the complete stepwise mechanism of the following reaction. Show all electron flow with arrows…

A:

Q: Consider the reaction scheme shown below. HCI [1] HO. (a) Provide a detailed mechanism for reaction…

A: This reaction will occur via 3 step. In first step protonation then Water molecule eliminate to…

Q: H3C. КОН, Н-О CH3 H

A: Organic reaction mechanisms SN1 reaction mechanisms.

Q: In an SNl reaction, among the three given alkyl halides below, [A_ I C[ is expected to

A: It is two step mechanism                     first step is formation of carbocation, it is slow…

Q: H2 in Pt ?

A: The process in which dihydrogen gas adds to alkenes and alkynes in the presence of catalysts like…

Q: 4. Propose a reasonable mechanism, using curved arrow notation, for the following reaction. Be sure…

A:

Q: Draw the product of the reaction shown below. Use wedge and dash bonds to indicate relative…

A: The product is given below:

Q: For the following dehydrohalogenation (E2) reaction, draw the major organic product(s), including…

A: E2 is a bimolecular reaction. The reaction involves one step mechanism in which the carbon –hydrogen…

Q: 3) Write a detailed mechanism of: CH, CH. HNO" H'SO O,N

A:

Q: 5. For the following reoction give a mechanism utilizing arrow notation for electron flow to explain…

A: In the given chemical reaction, formation of cyclohexanol is taking place. The chemical reaction is…

Q: (b) Consider the reaction of 1-bromobutane with a large excess of ammonia (NH3). Draw the reactants,…

A: The nucleophilic substitution reactions are the organic reactions, which involves the bonding of a…

Q: Give a clear handwritten mechanism and product for given below Sn2 reaction..a reaction shows all…

A: SN2 is reaction mechanisms:

Q: НО ОН NaBH4 Cl3C CląC H H,0

A: Trichloroethanol may be prepared by the direct reduction of chloral hydrate in water with sodium…

Q: Using curved arrow formalism, give the mechanism for the following reaction. Be sure to include…

A: Given,

Q: Which statement(s) is/are true regarding leaving Broups? L Weak bases make good leaving groups. II.…

A: I . ) Good leaving groups are weak bases. They're happy and stable on their own. Some examples of…

Q: 3. Show the reasonable curved mechanism for the reaction and make sure lone pairs Y Ocuk + Conc HBr…

A: (a) Lone pair of oxygen is acting as a HOMO and antibonding orbital of H-Br bond is acting as a…

Q: Rank the following carbocations in order of decreasing stability. Most stable

A: Carbocations are electron-deficient species that are formed by the removal of a hydrogen atom from…

Q: 1: NaOH 2: D;SO4 S-Methyl 3-methylbutanethioate

A: The reaction of carbonyl compounds with NaOH results in (SR) nucleophilic substitution reaction.…

Q: CH3 + НаС — сн н

A: We have to predict the mechanism for formation of given product via Michael addition.

Q: 1. MeONa, MEOH 2. H3O* workup

A: The goes via enolization at first then intramolecular SN2 reaction followed by quasi-favorskii type…

Q: 1. Which alkene is the major product of this dehydration?

A:

Q: H OH + H-CI = `CH, CH,

A:

Q: CH3OH (-HCI) CI ???

A: In this reaction lone pair of methyl alcohol attack at Carbon in which Cl is attached. Then Negative…

Q: Give the major product(s) of the following reaction. AICI, ? heat There is no reaction under these…

A: Given:

Q: Step 4: You have determined that one of the precursors is a vinyl halide, while the other is a vinyl…

A: Soln

Q: Carbocation rearrangement of the cation on the right gives: A) B) D) two of the above

A:

Q: "ropose a mechanism for the following reaction. но H,SO, + H,0

A:

Q: Rank the following carbocations in terms of stability from lowest to highest. to A B C D

A:

Q: (b) Show the mechanism of this reaction using proper arrow push notation. You mu intermediates,…

A: We will write the mechanism of the given conversion

Q: Complete each reaction sequence below by filling in the boxes for reagents and intermediate…

A: A pericyclic reaction follows concerted mechanism that proceeds through a cyclic transition state.…

Q: For the dehydrohalogenation (E2) reaction shown, draw the major organic product, including…

A:

Q: Give the mechanism (arrow-pushing) for the reaction below. NAOME/MEOH \Br b. Name the product of the…

A: The mechanism is provided below:

Q: + F2 >

A: Given is  Reaction of butane with fluorine in presence of sunlight.  We need to find potential…

Q: The first of the two heterolysis reactions below takes place readily, but the second one does not.…

A: Heterolysis reactions involves the breaking of bond in which two electrons in a bond distributed…

Q: Write o o mechanism to hronsform Compound A to B NH2

A: For reaction 1, we will use aniline (which is used as polymer)  For reaction 2 and 3, we will use…

Q: 4. For the Sn2 reaction below: Give the mechanism with curved arrows and products for the reaction…

A: Given:

Q: ) Make the following molecules, starting from a terminal alkyne and any alkyl halide, if needed. 8.)…

A: 8. A. At first 3-Methylbut-1-yne is treated with B2H6/THF followed by NaOH/H2O2…

Q: Add curved arrows to draw the first part of the mechanism: tautomerization of a ketone to an enol.…

A: A mechanism of an organic reaction is shown by the movement of electrons. An arrow is used to show…

Q: 3) Write a detailed mechanism of: CH CH. HNOT H'SO NO

A:

Q: 1) NaH 2) 3) H*, heat

A: NaH (sodium hydride) is a strong base. It abstracts a proton from more acidic hydrogen. The…

Q: CH3 CH, H3C-¢* + :Br: H,C Br : CH3 CH,

A: The movement of electrons are shown by curved arrows. There are two types of arrows to show the…

Q: Draw the major organic product generated in the reaction below. Pay particular attention to 1)…

A:

Q: why does this carbocation go through rearrangemnt by a hydride shift?

A:

Q: 1) NaOH H 2) H*, heat

A:

Q: CI H2N (-HCI) ??? NH2 2.

A: the reasonable mechanism for the reaction is

Q: 2) Rank these molecules by their SN2 reaction rate. If a difference in reaction rate is hard to…

A: The correct order of molecules towards SN2 reaction is   D > E > A > C > B.   The order…

Q: CH3 CH2BR NBS hv

A:

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.