1. Alcohol Substitution Reaction Mechanism: Draw the product for the substitution reaction below in the box. Then, draw the proper FULL electron-pushing mechanism for the reaction, including all intermediates (with formal charges and lone pairs of electrons) and all electron pushing arrows (is it SN1 or SN2?!). Label the electrophile and nucleophile in each step. а. Reaction 1: H-Br: .. HO. H20 A b. Reaction 2: H-Br: .. H20 A :он

Q: Ph. OTs OTs NaOH NANH, ? ? NaOH ? A В C Ph. CI NaOH dilute NaOH ? D

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Q: NO2 NH2 Br NO2 НООС b. NO2

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Q: Rank the following radicals from least to most REACTIVE: PH2 CI *AsH2 Why did you choose this order?…

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Q: D. Is the nucleophile strong or weak? E. Is the solvent polar protic or polar aprotic? F. What type…

A: Note: polar protic solvent and weak nucleophile and secondary alkyl halide all favors a sn1…

Q: Draw structures for the carbonyl electrophle and enolate nudeophlle that rea • You do not have to…

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Q: show all important steps of rxn. (3S,4R)-2-bromo-3-propyl-2- phenylpentane in ch3OH. label arrow,…

A: From the chemical structure, shown below, stereochemistry is not possible at 4th carbon. Therefore,…

Q: Determine the HOMO in the nucleophile and LUMO in the electrophile in the reaction below. NH, Me…

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Q: Provide the missing starting material(s), reagents, or products for each reaction as indicated by…

A: All the missing starting material, reagents or products are given in a attached image.

Q: For the following dehydrohalogenation (E2) reaction, draw the major organic product(s), including…

A: E2 is a bimolecular reaction. The reaction involves one step mechanism in which the carbon –hydrogen…

Q: Br HBr

A: available lone pair on O-atom acts as lewis base, H+ acts as lewis acid and lewis acid-base reaction…

Q: 1. Draw the structure of (4S)-1-bromo-4-methylhexane a. Draw the substitution product that would…

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Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…

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Q: CN- I"H Br

A: Alkyl halides can give nucleo phillic substitution reaction,in this case the given secondary alkyl…

Q: What is a major product of the reaction sequence shown in the box? of H. Mg H,0, HCI Brz or NBS ?…

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Q: Write down the mechanism for the nucleophilic asylum substitution reaction in Figure 40.

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

A: When one reactant is treated with a reagent then more than one reactive intermediate is formed. We…

Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…

A: We have to draw the curved arrow mechanism for the given reaction.

Q: II Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…

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Q: While we are at it, let's do the same thing for the second step of the mechanism. Again, what is…

A: In the second step of the mechanism, the enzyme accepts hydrogen from the conjugate acid of…

Q: Draw the mechanism ffrom benzaldehyde to this using:   i)NaBH4 ii)TsCl, py iii)NaCN iiii)H+,…

A: Given,  The mechanism for target product formed from benzaldehyde by using  i)NaBH4 ii)TsCl, py…

Q: While we are at it, let's do the same thing for the second step of the mechanism. Again, what is…

A: Answer

Q: Na O Select to Add Arrows NaOH Na O H. Br:

A: When atoms combine to make a compound, energy is always given off, and the compound has a lower…

Q: Rank these nucleophiles from best to worst Na- I -I Best (II)>(1)>(III) worst Best (1)>(III)>(II)…

A: A question based on introduction to organic chemistry that is to be accomplished.

Q: Why does the final product has the opposite configuration compared to the reactant? Shouldn’t it…

A: Here, the given compound is secondary alcohol. When, methylsulfonyl chloride (or mesyl chloride)…

Q: Drag the appropriate items to their respective bins. CH3 CH= CH2 CH3 CH3CH(CH3)CH,NH2 CH3CH2COO…

A: Attacking reagents can be classified into two types  Electrophiles (E+)  Nucleophiles (Nu-)…

Q: What major product (from Figure #1) results from the following dehydration reaction (from Reaction…

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

Q: For C, D and E, determine which step undergo the elimination, substitution or additor State the…

A: Given : We have to choose reagents for each step.

Q: Drawing the Product(s) of a Mechanistic Step. For the reactions that have TWO starting materials,…

A: Nucleophile: Donates pair of electrons to positively charged substrate resulting in the formation of…

Q: For each pair of reactants (A-C) draw all possible E2 products, label each as a mono, di, tri, or…

A: When an alkyl halide reacts with a strong base, the reactants can undergo two mechanisms. The…

Q: Rank the following substrates in order from slowest E1 reaction rate to fastest. Br Br Br Br A B

A: Given substrates,

Q: 3. Oxidation of Alcohols Mechanism: Draw the major product for the oxidation reaction below in the…

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Q: the major and minor products from the following reaction: (Draw the structure of all reactants and…

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

A: The cation that acts as a intermediate in the reaction is known as carbocation. In carbocation,…

Q: Question attached

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: For the substitution (SN2) reaction below circle the nucleophile and draw a box around the…

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Q: Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…

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Q: For the substitution (SN2) reaction below circle the nucleophile and draw a box around the…

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Q: In the allylic bromination with NBS below, a mixture of two products (A and B) can be formed due to…

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Q: final

A: Please find the file attached for explanation

Q: Add curved arrow(s) to draw the final step of the mechanism. 18rt Br 3-3 CH₂ H₂C Br H₂C

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Q: Part A: In the attached figure, rank the following compounds in order of their expected reactivity…

A: Compounds that has good leaving group more likely undergoes substitution reaction.

Q: Dtermine the Product A from the rxn Et H2O, H2SO4 A heat Co2Et CO2H Et а. b. С. d. Et `Et

A: The first step is the attack of water molecules to the ester carbonyl groups to give the carboxylic…

Q: Rank the following substrates in order from slowest SN2 reaction rate to fastest. Br Br Br H3C Br A…

A: SN2 stands for nucleophilic substitution reaction of order 2. In this reaction, the rate of the…

Q: Show how you might synthesize this compound from an alkyl bromide and a nucleophile in an Sy2…

A: The SN2 reaction mechanism involves the nucleophilic substitution reaction of the leaving group…

Q: In the molecules below, circle the carbon that will most likely have the electrophile attached to it…

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Q: Q2. For the reactions below, draw out the reactions as shown and answer the following questions for…

A: This reaction example of elimination reaction.

Q: • Circle the type(s) of reactions which would have rearrangements occur. SN1 SN2 El E2 • Propose a…

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Q: Draw the major product(s) of the following reaction. O, initiator • You do not have to consider…

A: Note : Alkene reaction with oxygen gives carbonyl compounds.

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.