SH [1] NaH a. [2] CH3B. b. CI S.

Q: Draw the products in each reaction. CH,CH3 CH;CH,OH K* -OC(CH,)3 а. Он CH3CH2O b. CH3-C-CH,CH3 d. CI

A: Since you have posted a question with multiple sub-parts, we will solve first three sub-parts for…

Q: Draw the products of each reaction. OH он CH3 Cl2 FeCla Cl2 a. b. С. FeCl,

A: The product of each reaction has to be drawn below. (a) (b) (c)

Q: Which molecules contain good leaving groups?

A:

Q: Classify each reaction as oxidation, reduction, or neither. a.

A: “Since there are multiple questions and it is not mentioned that which one has to be solved so I am…

Q: H OTos С. d. a. b. H OTOS H OTOS

A:

Q: Which SN2 reaction is each pair is faster? OBr O. OOCH3 Br A. OBr Br OCH3

A:

Q: Match each reaction with its correct energy diagram. Он OH H2SO4 H2SO4 HCI HO A) B) C) .......…

A:

Q: Draw the products of each reaction. [1] SOCI2 [2] (CH3CH2),NH (excess) SOCIl, a. b. он CH3CH2 HO

A: The product of the following reacts, (a) (b)

Q: Draw a stepwise mechanism for each reaction. a. OCH,CH3 HOCH,CH2CH,CHO + CH3CH2OH OH b. CeH;CHO CgHs…

A: (a) The compounds in which -C-O-C- bond is present are classified as ethers. The cleavage of ether…

Q: NH2 major product?

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Q: Of the choices, the predominant product is CH3 :Br-Br: NH ? FeBr3

A: The above reaction is an example of the elecorophilic aromatic substitution where the attaching…

Q: stereoisomers. NaOEt 1. Br NaOH Br 2. NaOtBu 3. A Меон 4. Br 2. Which reaction will proceed faster A…

A: 1) Elimination 2) SN2 reaction 3) Elimination  4) SN1 reavtion Reavtion B is faster than A due 1,3…

Q: draw each product

A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: Which halide is most reactive in SN2 reactions? Select one: CH2CH2CI ÇI CI H3C CI CI CH3

A: The reactivity order of SN2 : 1° > 2° > 3° alkyl halides.

Q: Draw the products of attached reaction.

A: In order to carry out the reaction and reach its final product we must know that LiAlH4 is a hydride…

Q: Draw the product of attached reaction.

A: Write the products of following reaction

Q: Draw the major product of the following reaction. 1. NaNH, 2 Br 3. H₂, Lindlar's catalyst

A:

Q: Draw the product of each reaction.

A:

Q: Label the α and β carbons in each alkyl halide. Draw all possible elimination products formed when…

A: The carbon to which the functional group is attached is called the alpha carbon. The next carbon to…

Q: Draw enol tautomer(s) for each attached compound ?

A:

Q: Which compound in each pair undergoes a faster SN2 reaction?

A: SN2 is a reaction in which attack takes place from back side, so less hindrance means faster or…

Q: What starting materials are needed to prepare each compound using a Michael reaction?

A: The reaction in which an enolate ion of one carbonyl compound undergoes conjugate addition reaction…

Q: Draw a stepwise mechanism for the following reaction.

A: 1.protonation of an alcoholic group in the presence of acid HBr Removal of water for the formation…

Q: Name each epoxide: CH3 a. (two ways) (two ways) CH b.

A: An epoxide is a cyclic ether consisting of one oxygen and two carbon atoms. During the IUPAC naming…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. CI 1. (CH3)2CULI (excess) 2.…

A:

Q: Name each epoxide: CH3 a. b. (two ways) H (wo ways) CHá

A: Answers are explained below.  Epoxides are named in three different ways those are oxiranes,…

Q: Draw the product of each reaction

A: Finding: To find the product of the following Reactions (a) & (b):

Q: Do ethers have a good leaving group ?

A: Ethers are the organic compounds which have the general formula R-O-R'. A group which leaves as a…

Q: What starting materials are needed to prepare each compound using a Heck reaction?

A:

Q: Label the a and B carbons in each alkyl halide. Draw all possible elimination products formed when…

A: Biomolecular elimination (E2) reaction: E2 reaction involves a one-step mechanism in which…

Q: Which compound can undergo Cannizzaro reaction? CH3CHO CHO

A:

Q: Draw the products of each reduction reaction.

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Q: CH3OH H2SO4

A: The reaction will undergo formation of Carbocation which will stabilize itself by expanding to form…

Q: Cl2, Hz0 .CI OH major product

A: Reaction of an alkene with halogen and water converts the double bond to a single bond and one…

Q: NH (e) Reagent(s):

A: The question is based on the concept of organic reactions.   We have to convert the reactant into…

Q: Draw the product of each reaction. [1] NaCN Br [2] LIAIH4 [3] H2O а. [1] DIBAL-H b. CEN [2] H2O

A: We have to predict the product of each of the reaction.

Q: Draw the product of each reaction. HBr CH;CH2OH а. С. H,SO4 [1] CH;O¯ b. [1] "CN d. [2] CH3OH [2]…

A:

Q: Which halide is most reactive in SNl reactions? Select one: CI CI H3C CI CH3 CH2CI CI

A: The SN1 reaction is a nucleophilic substitution reaction. It is a two-step reaction where the first…

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

A: The given reaction is reaction of a 2-bromopentyl cyclohexane reaction with NaOCH3, and the…

Q: Draw the products formed when each dihalide is treated with excess NaNH2.

A: a. The final product will be alkene if monohalide undergoes elimination, however, the final product…

Q: Draw enol tautomer(s) for each compound.

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Q: Draw the MAJOR product 1) Hg(OAc)2, H2O 2) NABH4 3) Na2Cr207, H2SO4, H2O

A: Given that : We have to draw the major product for the following reaction :

Q: Draw the products of each reaction.

A: Sodium amide (NaNH2) in presence of liquid ammonia acts as a very strong base. Chloro-benzene…

Q: What is the major product of this reaction? NaOEt HOET A. B. D. C.

A:

Q: Classify each reaction as oxidation, reduction, or neithe

A: The reaction in which the number of M-O bonds increases and the number of M-H bonds decreases, they…

Q: Draw the products formed when each dihalide is treated with excessNaNH2.

A: Given reaction,

Q: NaH d. C6H10O Br

A:

Q: Draw the Reactant Br2 (1 equiv) hv Br

A:

Reactive Intermediates

In chemistry, reactive intermediates are termed as short-lived, highly reactive atoms with high energy. They rapidly transform into stable particles during a chemical reaction. In specific cases, by means of matrix isolation and at low-temperature reactive intermediates can be isolated.

Hydride Shift

A hydride shift is a rearrangement of a hydrogen atom in a carbocation that occurs to make the molecule more stable. In organic chemistry, rearrangement of the carbocation is very easily seen. This rearrangement can be because of the movement of a carbocation to attain stability in the compound. Such structural reorganization movement is called a shift within molecules. After the shifting of carbocation over the different carbon then they form structural isomers of the previous existing molecule.

Vinylic Carbocation

A carbocation where the positive charge is on the alkene carbon is known as the vinyl carbocation or vinyl cation. The empirical formula for vinyl cation is C2H3+. In the vinyl carbocation, the positive charge is on the carbon atom with the double bond therefore it is sp hybridized. It is known to be a part of various reactions, for example, electrophilic addition of alkynes and solvolysis as well. It plays the role of a reactive intermediate in these reactions.

Cycloheptatrienyl Cation

It is an aromatic carbocation having a general formula, [C7 H7]+. It is also known as the aromatic tropylium ion. Its name is derived from the molecule tropine, which is a seven membered carbon atom ring. Cycloheptatriene or tropylidene was first synthesized from tropine.

Stability of Vinyl Carbocation

Carbocations are positively charged carbon atoms.  It is also known as a carbonium ion.