11. Give the mechanism of the following reactions. Make sure to show all electron lone pairs and formal charges on atoms and show the direction of electron flow using curved arrows. Br CH;CH=CH2 + HBr CH;CHCH;

Q: Treating 2-methyl-1-butene with methanol in the presence of sulfuric acid gives 2-…

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Q: 2. By using the same alkene, how do you synthesize the following alcohols? Give the alkene and show…

A: The formation of alcohol from the alkene with the same number of carbon atoms can be done by the…

Q: What is the functional group of the product of the reaction below? H3 C H2 ether ketone carboxylic…

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Q: HC=CH The synthesis above can be performed with some combination of the reagents listed below. Give…

A: For deprotonation of acetylene we need strong base such as NaNH2.

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: Complete these reaction. t CH= CH+ ZNa 2. HC = CH t 2Hz 3. CH2 CHz t cla 4 CH = CH t Oz

A: The answer to the following question is-

Q: Complete the following reaction by drawing a structural formula for the product. CH2CH, (1) NABH4…

A: Finding the product of the above reaction.

Q: Explain the Formation of a 2° carbocation and rearrangement ?

A: Carbocation are basically carbon as cations. These are having 3 bonds and incomplete octet. The…

Q: Draw a structural formula for the product of each SN2 reaction. Where configuration of the starting…

A: Given reaction,

Q: 20. C2 CH;OH 21. (1) O3 (2) (CH3)2S 22. CH;OH H,PO4

A:

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: b) Complete the following reactions of alkenes and alkynes by providing the structures of the…

A: ii) Alkynes react with Br2 molecules and form dibromo alkene first which again reacts with Br2 and…

Q: Write the products of the following reactions. If there is no reaction write NR. LDA +…

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Q: . Give the mechanism of the following reactions. Make sure to show all electron lone pairs and…

A: In this question we will give step-by-step mechanism by showing all the curved arrows, lone pair and…

Q: CH3 a) + HCI CH3 b) + Clz

A: The reaction in which hydrogen halide react with a double bond and gives addition product, is known…

Q: H. OH Step 1 Step 2 Step 3 16:18 21°C 2021/06/21

A: Hydration of alkene is done under acidic conditions. A carbocation is formed under this reaction. On…

Q: 4) Write structures for products. Pay attention to stereochemistry OH L OH TsC1 Pyridine TsCl =+…

A: Addition reaction is a chemical reaction involving the addition of two or more molecules to form a…

Q: Complete the following reaction by drawing a structural formula for the product. CH, 0 CH,CHCHCH +…

A: Catalytic hydrogenation of aldehydes :- Aldehydes on reaction with hydrogen in presence of finely…

Q: . Predict the product of this reaction 1-Cyclohexene + H2

A: PRODUCT :CYCLO HEXANE CYCLO HEXENE REDUCED IN PRESENCE OF Pd/C  TO FORM CYCLO HEXANE  DOUBLE BOND…

Q: Predict the product of this reaction 1-Cyclohexene + H2

A: Given reaction,

Q: Starting with acetylene and 1-bromobutane as the only sources of carbon atoms, show how to…

A: Introduction: Firstly, acetylene was treated with sodium amide and with 2 equivalent of…

Q: Functional Group Transformations? Starting Compound Typical Reagents Compound and Reaction Class…

A: Addition reaction involve combining two reactants to give a product. Addition of 2 equivalent of HX…

Q: Conversion of 2-methyl-2-butene into a tertiary alkyl halide. OBra. H0 O HBr, ROOR O Bra, ROOR HBr

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Q: Rank these cyclohexane rings in terms of increasing energy. OH -HO- O- OH IV V II II

A:

Q: Predict the organic products of the reaction of 2 butene with each reagent. Be sure to indicate…

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Q: Starting with acetylene and 1-bromobutane as the only sources of carbon atoms, show how to…

A: In the first step, acetylene and 1-bromobutane reacts with each other in presence of a strong base…

Q: Br Br NaNHz KH 200 0 =

A:

Q: The addition of BH3 to an internal alkyne followed by CH3COOH yields: An aldehyde O A ketone O A…

A:

Q: Show how to convert 4-methyl-1-pentene to the compound shown here. NH₂

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Q: (a) Which carbonyl compounds would CH3 CH3CH,CH2CH,CCH,OH (b) HyÇ OH (e) you reduce to produce the…

A: The compounds given are,

Q: Complete these nucleophilic substitution reactions. In each reaction, show all electron pairs on…

A: SOLUTION: Step 1: The reaction of n-butyl bromide with sodium methoxide gives methyl propyl ether as…

Q: Start with methylcyclohexane to prepare cis-1,2-dihydroxy-1-methylcyclohexane in 3 steps

A: Usually, the cis hydroxylation of a double bond is done by using OsO4 , followed by NaHSO3 and H2O.…

Q: Reaction of hbr with 2-methylpropene yields 2 bromo 2 methylpropane. What is the structure of the…

A: The reaction of Alkene with HBr  gives Bromo product.       In this reaction carbocation is formed…

Q: Please name the following compound. (3S, 10S,Z)-10-((S)-sec-butyl)-3-methyltetradec-7-ene (3S,…

A: The naming of any compound is done by the number of carbon atoms present in parent chain and the…

Q: Predict the products of the following reactions.  2-ethoxy-2-methylpentane + concd. HBr, heat

A: 2-ethoxy-2-methylpentane + concd. HBr, heat would lead tp cleavage of ether leading to formation…

Q: O Give the reaction mechanism showing all possible products for the following reaction (a) Reaction…

A:

Q: Draw a structural formula for the product of each SN2 reaction. Where configuration of the starting…

A:

Q: CH3 CH2 CECCH2 CH3+ H20 ?

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Q: The Wolff-Kishner reaction involves the reaction of an aldehyde/ketone with hydrazine in the…

A: The Wolff-Kishner reduction is a reaction used to convert carbonyl functionalities into methylene…

Q: The product of the reaction sequence BH, H202. OH b. HO, enone of the above BH

A:

Q: Ph Ph CH3 Ph CH3 The Wolff-Kishner reaction involves the reaction of an aldehyde/ketone with…

A: The mechanism for the first step that is nucleophilic addition is shown below,

Q: What products would you expect from the following halogenation reactions?(a) 2-Methylpropene + Br2…

A:

Q: Complete the following nucleophilic substitution reactions. In each reaction, show all electron…

A: Given:

Q: 7. a. Which categories/classes does this compound belong to (for example, aldehyde, ketone)? b. Use…

A: First belongs to thiol family. Second  belongs to ketone  family  .

Q: Draw structural formulas for all alkenes that could bê üsed to prepare the aleonol SHOWIH Delow OH…

A: Oxymercurattion reaction: The reaction takes place in 2 steps. Step 1: The alkene reacts with…

Q: .Acidication of triphenylmethanol generates a red-coloured carbocation H20 LOH2 HO ? Use curly…

A: At first -O-H group undergo protonation to give better leaving group -OH2^+. It cleaves to give…

Q: Complete step 1 of this reaction. Include lone pairs and charges in your drawings. Using wedges and…

A: Here HCC- acts as a nucleophile and attacks the electron-deficient center.

Q: CH3 Heat H2/Ni t) HO CH2 CH20H, HA 2) Ni/H 3) Hg O* LIAIH4

A: Please find the attached sheet.