CH3 CH,CH3 CHз CH;CO CH;CH,O CH;CH,CO CH;CH,CO ČH,CH3 1. ČH3 1. 1. ČH3

Q: Why is ethanol a better nucleophile than tert-butanol?

A: Alcohol can be defined as an organic compound in which hydroxyl group is attached to carbon atom.

Q: Which is the most stable: 3,4-dimethyl-2-hexene, 2,3-dimethyl-2-hexene, or 4,5-dimethyl-2-hexene? a.…

A: The stability of an alkene increases as the number of alkyl substituents bonded to its sp2 carbon…

Q: For alkenes A, B, and C: (a) Rank A, B, and C in order of increasing heat of hydrogenation; (b) rank…

A: Alkenes are the unsaturated hydrocarbons with at least one double bond between carbon atoms of the…

Q: Consider the reaction of (R)-2-chloro-3-methylbutane with sodium iodide to form a product. (a) Draw…

A: We have find out reaction scheme. Note -As per our company guidelines we are supposed to answer only…

Q: H,C -CH3 H,C CH3 H,C -CH3 CH structure 1 structure 2 Which is the more stable alkene? Explain your…

A: Stability of alkene depends on 1. Hyperconjugation conjugation 2. Resonance or mesomeric effect 3.…

Q: The reaction below is commonly used as a laboratory preparation of cyclohexene. The Forward and…

A: Chain termination step is the last step of free radical mechanism.in this step, free radicals react…

Q: When 2-bromo-2,3-dimethylbutane reacts with a strong base, two alkenes (2,3-dimethyl-1-butene and…

A: An E2 reaction is a concerted, one-step reaction in which the proton and the halide ion are removed…

Q: 6. What kind of reaction does the conversion of A to B represent? H2SO, H20 но н A в A) Acid-base…

A:

Q: What is the best set of reagents to use for the synthesis?

A: Wittig reaction: It is very useful reaction in converting carbonyl compounds into alkenes. The…

Q: 5. a) Determine the major product that is formed when the alkyl halide reacts with a hydroxide ion…

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Q: N-Chlorosuccinimide (NCS) serves as a source of Cl+ in electrophilic addition reactions to alkenes…

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Q: Which reagent is appropriate for the following reaction yclohexene converted to trans-cyclohexane…

A:

Q: Draw stepwise mechanisms for the following. Use arrows to show movement of electrons and draw all…

A: Ketone formes enol in presence of acid or base

Q: What alkane is needed to make each alkyl halide by radical halogenation?

A:

Q: Figure 10 1 BH3 CH, OH 2 H202, NaOH CH3-CH-CH-CH3 A в CH3 CH2 CH3-C-CH2- CH3 CH2=C-CH2-CH3 D CH3 CH3…

A: Which alkene is required to complete the reaction in Figure ?

Q: following reactions is a net on Carbon The 9) addition b) rearrangement c) elimination d…

A: In this question, we have to choose the correct option for the given reaction.

Q: N-Chlorosuccinimide (NCS) serves as a source of Cl+ in electrophilic addition reactions to alkenes…

A: Since alkyne is a nucleophile. hence the Cl+ produced by the N-Chlorosuccinimide will be attacked by…

Q: a. Identify two alkenes that react with HBr to form 1-bromo-1-methylcyclohexane without undergoing a…

A:

Q: In each case tell which SN2 reaction will proceed faster. 1. The displacement by I- on (a) CH3Cl or…

A: As the ability of leaving group increase rate of SN2 reaction will be increase Stability of leaving…

Q: a) reaction of 1-butene with Cl2/H2O b) reaction of 1-butene with H+/H2O c) reaction of…

A:

Q: This compound was synthesized from benzene by the scheme outlined. CH3 Br ČH3 1. CH3CI, AICI3 2.…

A: The first step of this synthesis is called Friedel craft alkylation . It is an electrophilic…

Q: The reaction of 2-methylpropene with HBr in ether is described below. Answer the following questions…

A: Given reaction is :  Which product is the anti-Markovnikov product = ?

Q: b H3C CH3

A: The reaction of an alkene with an acid is termed as halohydrogenation, which includes the breaking…

Q: 1) H Br2 Mg в 2) Hо A FeBrg РСС но OH E (H*), -H20

A:

Q: 4. Give the possible reagent or major product for the following reactions: a. он + product A +…

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Q: Rank the alkyl halides in order of increasing E2 reactivity. Then do the same for E1 reactivity.

A: The factors that influence the order of ( E1 and E2 ) elimination reactions are:  1) The reactivity…

Q: 5. a) Determine the major product that is formed when the alkyl halide reacts with a hydroxide ion…

A: In elimination reaction the leaving group is removed along with beta-H atom, when the substrate is…

Q: A. The Cycloheptatrienyl cation is very unstable although it has seven resonance structures, however…

A: Conditions that a compound must satisfy for being aromatic are: Must be cyclic and planar Must have…

Q: What is the major product of a reaction between I – Cl and 2-methyl propene in CH2Cl2?

A: Reaction name : Electrophilic addition reaction.  Electrophile: I+ (idonium ion)  Intermediate:…

Q: formula for a carbocation

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Q: Draw the major products obtained from the reaction of one equivalent of HCl with the following…

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Q: Which is the method of choice for preparing the ether (CH3CH2),COCH3? (a) (CH3CH2), COH + CH3MGBT…

A: Since you have asked multiple questions, we will answer only first question for you. In order to get…

Q: Reaction of (CH3)3CH with Cl2 forms two products: (CH3)2CHCH2Cl (63%) and (CH3)3CCl (37%). Why is…

A: The reaction via which one halogen group is added to the compound is termed as halogenation…

Q: 7. What alkene should be used to synthesize 3-bromohexane? Br ? + HBr CH,CH,CHCH,CH,CHI

A: Hey, since there are multiple questions posted, we will answer first question. If you want any…

Q: 1. HBr is a by-product of reaction of alkenes with bromine (electrophilic addition) 2. Alkynes have…

A: For the above given statements "true" and "false " Can be predicted by explaining the statements in…

Q: 2. Draw the reactantls) CH3(CH2)24 C-o-CH2 CCH2)48 CH3 t HzO insect wax

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

Q: Ketone A can be converted to alkene B in a one-step reaction via route I. It can also be converted…

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Q: 3. Supply the starting material, reagent/condition, or major product to complete the reaction below.…

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Q: Explain why the addition of HBr to alkenes A and C is regioselective, forming addition products B…

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Q: 8. Choose the most stable alkene from each group: a. b.

A: Note: According to our guidelines we are supposed to answer only first question

Q: NAL NEL NIL NOL 7. an E-alkene 8. has the most negative heats of hydrogenation 9. the most stable…

A: The alkenes given are,

Q: 9) For the reaction between isopropyl 1-propyl (or 'n-propyl') ether and HBr, what are the expected…

A: option A

Q: Why is 5-octene not possible? 2. Why is 3,3-dimethyl-3-octene not possible?

A:

Q: Which SN2 reaction will occur most slowly? (Assume the concentrations and temperatures are all the…

A:

Q: (a) Octane burns with oxygen gas. (b) 3-ethylpentan-2-ol is combined with an oxidizing agent, H2O2.…

A: a) Octane burns with oxygen gas. The equation for the given reaction is, 2C8H18 + 25O2 ---> 16CO2…

Q: What is the leaving group in the following reaction (Figure 8)? SH2 SH HI

A: Reaction  It is a process in which reactant molecules react to each other and form another molecule…

Q: 3 Organic Chemistry, helppp with ALL PARTS(A&B) Consider the monoterpene linalool, a natural product…

A: When alcohol treated with strong protic acid, such as sulfuric or phosphoric acid then dehydration…

Q: H,C -CH CH CH H,C: CH structure 1 structure 2 Which is the more stable alkene? Explain your answer.

A: A question based on alkene that is to be accomplished.

Q: 1. Which will be the major product if 3,3-demethyl-2- butanol to react in 85% of H3P04? a.…

A: Alcohol gives dehydration reactions when they react with a strong acid like H2SO4 or H3PO4 to form…

Q: If you react 0.15 mol of 2-methylcyclohexanol, what is the theoretical yield in moles of…

A: Reaction of 2-methylcyclohexanol to yield methyl cyclohexene is given as:

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.