1. aq. NaOH reflux NaCI H20 он 2. HI a = Proton transfer d = Radical chain addition g = E2 Elimination b = Lewis acid/base e = Electrophilic addition h = SN1 Nucleophilic substitution C = Radical chain substitution f = E1 Elimination i = SN2 Nucleophilic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1.

Q: 1. HC-C: u 2. a = b = E2 Elimination Electrophilic addition c = SN1 Nucleophilic substitution HC CH…

A: 1- d2- bExplanation:Step 1: Step 2: Step 3: Step 4:

Q: EX→DUU Step 1: Nucleophilic addition of hydroxide ion to the ester carbonyl group A INFRARR H3C.…

A:

Q: 1. DMSO Br K CN CN KBr 2. OEt Na OEt Ot HOET Na* a = Proton transfer b = Lewis acid/base c = Radical…

A: The reactions given are,

Q: Choose the reaction conditions to complete the acid-base reaction shown. NaH CH3CH2OH H C:O A B C D…

A: Hex-1-yne is given, hydrogen on triple bond will act as strong acid, we can use strong base to make…

Q: OH 1. Na OEt CH3OH Br Br2 HBr ÓCH, d = Radical chain addition e = Electrophilic addition a = Proton…

A: Given are two organic  reactions.

Q: DMSO /HO. N-H KOBu KB HO-BU a- Proton transfer g-Syl Nucleophilic substitution h- Sy2 Nucleophilic…

A: Answer 1 :- (d) Electrophilic addition    N-Bromosuccinimide or NBS is a chemical reagent used in…

Q: 1. CI AICI 2. H₂SO OH H.C a = Proton transfer b = Lewis acid/base c = Radical chain substitution d =…

A:

Q: HO pyridine 1. SOCI2 SO2 2. H2SO4 O-H HSOA a = Proton transfer d = E1 Elimination f= SN1…

A: The proton transfer reaction involves the removal of a proton (H+) from one species and the addition…

Q: 1. NaOH HBr H20 Br 2. Ph Ethanol H3C. -Ph КОн Ph KCI H20 H. CI a = Proton transfer d = Radical chain…

A: In this question, we will Identify the type of mechanism ( means name of Mechanism ).  You can see…

Q: 1. 2. CH3 1. tom 2. aqueous H₂SO4 a Proton transfer b = Lewis acid/base c = Radical chain…

A: Conversion of alkene into alcohol is an example of electrophilic addition.Conversion of alcohol into…

Q: Identify the mechanism by which each of the reactions above proceeds from among the mechanisms…

A: Organic chemistry is branch of chemistry in which we deal with organic reaction. Organic reactions…

Q: Indicate the major organic product that would be formed under the conditions below: 1. ВН3 THF 2.…

A:

Q: Br 1. Br2 Br 2. Br + KBr + HOCEt3 a = Proton transfer b = Lewis acid/base e = Electrophilic addition…

A: Let's break down each reaction into its parts so that we can figure out the mechanism for each given…

Q: ||| Rank these alkyl halides in order of increasing reactivity in an SN2 reaction. CI A) ||| < | <…

A: •Reactivity in SN2 reaction:- Reactivity for SN2 reaction is depend upon steric hinderence. •More…

Q: A set of three nucleophilic displacement reactions is shown below: CH3 SOH CH3CH2CCH3 SN1 reaction…

A: The replacement of any atom or group of atoms by a nucleophile is termed as nucleophilic…

Q: 1. ✓ OH + HCI OH 2. K CN Br a = Proton transfer b = Lewis acid/base c = Radical chain substitution…

A: Step 1: In SN1 first carbonation generated then nucleophile attack Here OH is not good leaving group…

Q: 1. OH HBr 2. H3C-O + H3C-O-Li LOH2 Br a = Proton transfer b = Lewis acid/base d = E1 Elimination e =…

A: 1. In the first reaction the oxygen group of the cyclohexanol acts as a base and abstract the proton…

Q: AS-5. The electrophilic aromatic substitution reaction is exothermic. Which potential energy…

A: Ans: Option A.

Q: 1. 2. NaOH e H₂C-1 H₂C OH a Proton transfer b = Lewis acid/base c = Radical chain substitution…

A: To determine the mechanisms through which the reactions take place.

Q: for of 1. conc. HBr OH H2O 2. Br, Br. HBr d = Radical chain addition g = E2 Elimination h = SN1…

A:

Q: a = Proton transfer d = Electrophilic addition g = SN1 Nucleophilic substitution b = Lewis acid/base…

A: The solutions are

Q: NH₂ N-Br + DMSO/H₂O NH₂ Br 2. Br₂ HBr NO₂ NO₂ a = Proton transfer e Electrophilic addition h = SN1…

A: Alkene with NBs/ water undergo cyclic bromonium ion Benzene with br2 undergo substitution reaction

Q: Question 6 Give the major mode of reaction for primary alkyl halides O E1 O SN2 O E2 O SN1

A:

Q: None

A: To rank the nucleophiles in order of increasing strength, we need to understand the nucleophilicity…

Q: q, a Proton transfer d = Electrophilic addition g = S 1 Nucleophilic substitution b = N 'N' Lewis…

A:

Q: n-Bu Na NH2 1. -CN CN 2 Br NaBr NH3 toluene, reflux n-Bu OH Aqueous acetone 2. H20 HBr optically…

A: The first reaction is a double alkylation of a nitrile compound.  The second reaction is a…

Q: Can you answer this question? Identifying the reaction mechanism

A:

Q: LAF

A: 1) SN2 nucleophilic substitution ( Option - i) 2) SN2 nucleophilic substitution (Option- i)

Q: 1. CH3 OCH3 Aqueous HO,S- -CH3 methanol OEt OEt NaBr 2. Na a = Proton transfer d = Electrophilic…

A: Given are two organic reactions.

Q: ab² + H=BC: •Where are the curved arrow pushing mechanism as well as the non-bonding electrons. What…

A: Given that, a reaction scheme is shown below We have to draw the curved arrow reaction mechanism…

Q: Find out the order of following reaction: 2NO₂ → 2N0 +0₂ H₂+1₁₂→ 2HI - H2C12 (hv) → HCL C12H22011 +…

A: ( If you have any questions related to this problem please feel free to ask me).

Q: 1. Na toluene reflux + NaCl .OH H₂O + 2. Br2 Br. HBr a = Proton transfer d = Radical chain addition…

A: Step 1: Explanation for Reaction 1 :      Sodium phenoxide (NaO) is a potent nucleophile that has…

Q: = Proton transfer d = Electrophilic addition g = SN1 Nucleophilic substitution b = Lewis acid/base e…

A: check in image

Q: Identify the mechanism by which each of the reactions above proceeds from among the mechanisms…

A: In first reaction OH is added into the carbon atom of cyclopentene , H2O behaves like a nucleophile…

Q: 1. Ph NME2 H2SO4 Ph HO, Ph NM22 NME2 Ph Ph Ph Tamoxifen anti (brest) cancer drug OH2 Br 2. HBr a =…

A:

Q: to . 1. H20 HO, + conc. HCI 2. OH NaHCO3 H20 CO2 Nal + + a = Proton transfer d= Electrophilic…

A:

Q: 1. Br Na NaBr Ph 2. CI NaOH но d = Radical chain addition g = E2 Elimination h = Sy1 Nucleophilic…

A:

Q: How to attempt this problem?

A: (1)The first reaction is Lewis acid/base reaction.

Q: How to attempt this problem?

A: (1) The hydride act as strong Lewis base which abstract the proton from alcohol; hence, the reaction…

Q: H Ph 1. .CI NaOH Но Ph Br DMSO / H20 2. N-Br ..OH N-H a = Proton transfer d = Radical chain addition…

A:

Q: EtOH 1. + NaQEt [Review Topics] [References] NaCl HOEL 2. Br Acetone + Nal a = Proton transfer b =…

A: 1. Option a: Incorrect. The reaction does not only involve proton (H+) exchange from one molecule to…

Aromatic Compounds

Aromatic organic compound or aromatic system is an important class of hydrocarbons under the branch of organic chemistry. Aromatic compounds are also called arenas. The definition of aromatic organic compounds can be stated as a class of organic compounds with a planar cyclic ring of atoms bonded through alternated single and double bonds. Due to these alternating bonds, a peculiar feature termed as ‘resonance’, that is, delocalization of pi electrons or the electrons is shared within the atoms of the ring which are present in the aromatic compounds. The word ‘aromatic’ includes a Greek word ‘aroma’ which means smell, indicating that they were named as such due to the sweet odor they produce. Many well-known flavors such as vanilla, cinnamon, and few scents from flowers are extracted from aromatic compounds. Benzene with chemical formula C6H6 is a very common aromatic compound that contains six atoms of carbon held in the cyclic ring of alternate double bonds. It is also to be noted that not all aromatic compounds contain benzene ring. This can be explained by Huckel’s rule.