CI I A. II B. I C. IV D. III CI NH₂ NaNO₂ + HC1 273-278K II CI N,CI III Cu₂Cl₂ Y + N₂ Cl IV

Q: Click the "draw structure" button to launch the drawing utility. What alkene is the major product…

A:

Q: Label attached pair of compounds as keto–enol tautomers or constitutionalisomers, but not tautomers.

A: Constitutional isomers are the isomers having same molecular formula but different bonding patterns…

Q: base-catalyzed halogenation of acetone, how do you explain why the second and third halogenation…

A: Acetone have acidic hydrogen and OH- is base so acid-base reaction takes place

Q: A mechanism pattern involved in this reaction is: O- rearrangement loss of a leaving group…

A:

Q: Which statement is true? Bromination is faster than chlorination because the rate-determining step…

A: Asking is, In Given statement choose the true one?

Q: 4) For the following reaction map, provide the products, or reagents/ direction of the reaction…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: 3. Draw the structures of compounds X and Y in the box provided. Me 1. Dihydroxylation 2. HIO4 OH…

A: In the given reaction, one compound reacts to form two products i.e., compound X and compound…

Q: OH conc. H₂SO4 heat ?

A:

Q: Br. CH3ONA H

A: The conformer structure for given structure is shown below.

Q: # of stereoisomeric products?

A: The products are given below -

Q: Draw ALL products of the following reaction, then upload all drawings to the question at the end. N

A: Given is organic reaction.In which reactants are amine and acid chloride.

Q: Explain why A is a stable compound but B is not.

A: Introduction :  We have to tell which compound is more stable.

Q: Draw the products of attached reaction. Include all stereoisomers formed.

A: The product of given reaction can be drawn as,

Q: 1) CH3CI, AICI 2) 3 mol NBS ? Modify the given copy of the starting material to draw the product.

A: Friedel-Craft alkylation reaction: When the benzene reacts with an alkyl halide in presence of Lewis…

Q: Draw the alkene that would react with the reagent given to account for the product formed. ? + H₂O…

A: Addition of water to alkene: Water adds to alkene to form alcohol. The addition of water is…

Q: Draw the two major products obtained in the reaction shown. CH2C12 Br2 (one equivalent)

A: 1,2-Addition involves the formation of a single product where the added group is attached to the…

Q: Explain how this epimerization reaction occurs. H3C H3C H i) CH3ONA/E1OH ii) H30" ČH3 CH3

A: To explain how  the epimerization reaction occurs

Q: Br "cEN,

A: Cyanide ion is a weak base and a strong nucleophile. So, It will react with 2-bromocyclohexanone via…

Q: OMe OMe H2SO4 2 equiv. OMe OMe

A: Given reaction is : Draw an arrow pushing mechanism and explain why less than two substitutions are…

Q: 2. Draw the stepwise mechanism of the following reaction. OH -CH3 H₂SO4 -CH₂ -CH₂ CH₂

A: Given a cyclopentanol and reagegent H2SO4 . Draw the stepwise mechanism.

Q: ОН K2Cr2O7 H₂SO4

A:

Q: A B

A: This is an elimination reaction.  Here HCl is removed or eliminated to get an alkene.

Q: Draw all products, including stereoisomers, in attached reaction.

A: Draw all products, including stereoisomers, in the attached reaction.

Q: ОН

A: These reactions are generally proceeds in a heating or light conditions.  Here we are given with…

Q: ||

A:

Q: Draw all stereoisomers formed in attached reaction.

A: The given is the formation of cyanohydrin which is a nucleophilic addition. the given reaction…

Q: When a carbonyl compound is attacked by a nucleophile resulting in the formation of a new…

A: In the carbonyl compound nucleophilic addition reaction occurs.

Q: Which compound is the major product of the reaction shown below? Oso4, tert-butyl peroxide tBuOH/HO…

A: Osmium tetroxide gives syn addition product with 1,2-dimethyl cyclohexene.

Q: Which of the following statements is FALSE about pericyclic reactions? * Pericyclic reactions occur…

A:

Q: Draw both resonance structures of the most stable carbocation intermediate in the reaction shown.

A: The intermediate of the given reaction is a carbocation. In carbocation, carbon carries a positive…

Q: (a) Add curved arrows for each step to show how A is converted to the epoxy ketone C. (b) Classify…

A: (a)  In this particular mechanism first the peroxide ion undergoes 1,4-addition with the reactant A…

Q: The Markovnikov product resulting from an addition reaction to an unsymmetrical alkene is formed…

A: -> In markovnikov's addition reaction reaction proceeds through formation of the most stable…

Q: Draw all the enol tautomers for each of the ketones

A: The enol form has a structure containing a carbon – carbon double bond and a hydroxyl group.