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

Q: b. Draw the FULL electron-pushing mechanism for the reaction depicted including ALL intermediates…

A:

Q: B. CIRCLE (CROSS-OUT) the FASTEST (SLOWEST) Nucleophilic Substitution Br + H3C-O + H3C-O .CI

A: Rate of Nucleophilic substitution depends on the nature of leaving group. Better the leaving group…

Q: v.. Using curved arrow notation, propose a detailed mechanism that is plausible for the following…

A: This is an example of formation of bromonium ion followed by intramolecular SN2 reaction.

Q: Show the full curved arrow mechanism for the following reaction, clearly showing how the indicated…

A: The first step of the reaction involved the elimination of Br- (bromide) ion to generate a 2o…

Q: Draw curved arrows for the following reaction step. Arrow-pushing Instructions CH3 CH3 H-0-H H3C-C+…

A: This is SN1 reaction  When tertiary butyl chloride reacts with water forms carbocation and gives…

Q: Draw the major product of the following reaction and enter its InChI code in the space provided. OCH…

A: In this question we have to tell the major organic product of the reaction.

Q: Draw a stepwise, detailed mechanism for attached reaction.

A: A detailed mechanism for the given reaction can be drawn as,

Q: 1. NABH4 CI 2. H,O

A:

Q: Draw a complete mechanism for the following reaction. Be sure to start with the formation of the…

A:

Q: 1. Draw a complete, arrow-pushing mechanism that shows the product from each of the following…

A: “Since you have asked multiple questions, we have solved the first question for you. If you want any…

Q: Draw a detailed mechanism for the following reaction, clearly showing all electron movement NH H*,…

A: Treatment of imine with water leads to formation of ketone/aldehyde . This reaction is called…

Q: HBr "SN1-like" H :0. :Br: H 2° alcohol 3° alkyl bromide

A: Given reaction follows Sn1 mechanism.

Q: Br2 CH3OH

A: Organic reaction mechanisms

Q: an you explain the full mechanism for this transformation

A: The aromatic substitution of hydrogen with deuterium occurs on reacting benzene with deuterated…

Q: Draw a step-wise mechanism for each of the following reactions. Show all arrows, proton transfers,…

A:

Q: Draw all products, including stereoisomers, in the following reaction.

A: The given reactant is a 3° (tertiary) alkyl halide.

Q: CH,OH OH + CO2 H. OH H ОН OH ČH,OPO,2 ČH,OPO,2

A: First aldehyde to carbo

Q: Give the curved arrow mechanism for the transformation below CI H2N-NH2 NH pyridine NH

A: The answer is given as follows

Q: 3. Draw a detailed arrow pushing mechanism for the following reaction H i. Og, ii. PPH3 CH2CI2 H

A:

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

A: Given the first step of this reaction is the electrophilic addition of deuterium (D).  Second step…

Q: 3) Give a complete, detailed mechanism for the following transformation. C, HCI HCI

A:

Q: 5. Draw a detailed arrow pushing mechanism for the following reaction. Is the rate-determining step…

A: When No carbocation is formed then reaction is SN2.if carbocation is formed then reaction is SN1

Q: Draw out the complete mechanism of the reaction and include all relevant electrons and arrows…

A: It is given that in the reaction benzaldehyde and acetone are the substrates which are undergoing a…

Q: :ÇI: CH3 + KOTBU H,C ČH3

A: Here, strong base/nucleophile is present, so there is a possibility of substitution as well as…

Q: Draw a stepwise, detailed mechanism for the following intramolecular reaction.

A: SOLUTION: Step 1: The intramolecular ring closure is carried out in the presence of strong acid like…

Q: CH3 CH3 CH3 CH3 CH3 H3C Y

A: Interpretation -  To complete the mechanism of the reaction starting from the intermediate  X, by…

Q: Using Curved Arrow Formalism, draw the reaction of 1-methylcyclopentanol treated with aqueous…

A:

Q: Draw the mechanism for the following reaction. Be sure to include all curved arrows. HO-S-OH OH H20…

A:

Q: 3/5 5.1 each indicated reaction. Mechanisms. Using curved arrows, suggest a reasonable mechanism for…

A: The reaction of alkene with phosphoric acid leads to the formation of carbocation. The oxygen of -…

Q: Draw the mechanism for the following reaction:

A: Please go through the reaction mechanism.

Q: Draw curved arrows to show electron reorganization for the reaction step below. Arrow-pushing…

A:

Q: Draw the complete mechanism for this reaction. p-CH3- CgH4– SO;H + H3C-OH

A: The organic conversion helps in the conversion of one organic compound into other compounds. This is…

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 the curved arrow mechanism for this reaction including the charges where necessary CO,Me N…

A: Electrophilic aromatic substitution is an organic reaction in which an atom that is attached to an…

Q: CH3 :Br: C=C H -Br: H -C C- -CH3 H. H. H. Add curved arrows for the first step. Draw both the…

A:

Q: The E2 Mechanism Draw the major and minor elimination products for the reaction of…

A:

Q: The following transformation is an example of a Darzens reaction. Draw its complete, detailed…

A: The Darzens reaction is an organic reaction that takes place between an aldehyde or ketone and an…

Q: Could the reactions shown here take place by a concerted mechanism?

A:

Q: Br2 H20 CH3CH,CH,CCH,Br CH,CH,CH,C=CH

A: The mechanism of the following reaction is as follows:

Q: 9. Draw a complete, detailed mechanism for the reaction below, and product(s). CH,OH NaOCH3

A: Ester are derived from substitution reaction of carboxylic acid and an alcohol, they are volatile…

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: Draw a curly arrow mechanism to clearly describe why the following reaction gives a trans dibromo…

A: Reaction of alkenes with bromine results in the formation of vicinal dibromides i.e. 1,2-dibromides.…

Q: CH,0-P-8 OCH, CH;0O, NaOCH3 H. OCH3 + CH,0 OCH3 CH;OH CH;0 CH;0

A: This is an example of Wittig-Horner reaction

Q: Draw the structure of all products of the mechanism below. H-C=C -OH + H-Ö-CH, H. it

A: Due to presence of lone pair electrons in the O atom, alcohols like methanol can act as nucleophiles…

Q: Draw the product by following the curved arrows. This reaction is an example of a [3,3] sigmatropic…

A: Sigmatropic rearrangement is shifting of sigma bond with the reorganization of pi-bonds in a system.…

Q: Draw the complete, detailed mechanism (including curved arrows) for each of the following reactions…

A:

Q: Draw a stepwise, detailed mechanism for the following intramolecular reaction.

A: The intramolecular ring closure is carried out in the presence of strong acid like H2SO4. The acid…

Q: H3C Br HBr H3C-C=C-CH3 c=C CH3

A: GIven The reaction involves addition of HBr to symmetrical alkyne. Since the alkyne is symmetrical,…

Q: Draw curved arrows to show electron reorganization for the reaction step below. Arrow-pushing…

A: HO- is a nucleophile and it shows tendency to attack in electron deficient center of any compound.…

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.