Days 3 and 4: photocycloaddition OH 8.00 + N. OH Resorcinol trans-4,4'-bpe 1. Co-crystallization 2. UV light 3. NaOH extraction N H + Resorcinol

Q: You have learned two ways to make an alkyl benzene: Friedel–Craftsalkylation, and Friedel–Crafts…

A: Alkyl benzenes are the substituted benzene in which substituent is an alkyl group. Benzene undergoes…

Q: Information about the mechanism of the reaction undergone by a series of substituted benzenes can be…

A: a.

Q: O OMP

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Q: For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be…

A: The reaction mechanism SN1, SN2, E1 or E2. SN1 and SN2 are nucleophilic substitution reaction by…

Q: a) Describe the general steps in the mechanism for an SN1 reaction and an SN2 reaction. b) Discuss…

A: The reaction in which an atom or group is substitutes by any other atom or group is known as…

Q: Friedel-Crafts alkylation can be difficult to control. What are some of the experimental methods…

A: The three key limitations of Friedel-Crafts alkylation are: Carbocation Rearrangement - Only…

Q: a) The radical chlorination of pentane is a poor way to prepare 1-chloropentane but radical…

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Q: Label the reactive features of the following reactants, select the most reactive feature, then write…

A: The reaction in which unsymmetrical alkene is reacted with HBr in presence of peroxide is known as…

Q: Q1) why the radicals are stable when they are next to either electron with_drawing groups or…

A: Free radicals are generated by homolytic cleavage of a sigma bond These are e- deficient species…

Q: Which of the following molecules reacts faster with NBS? Explain using mecha reasoning with…

A: The objective of the question is to apply Hammond's postulate to predict the relative reactivity of…

Q: One of the following Diels-Alder reactions will occur more rapidly than the other. Draw the major,…

A: The answer is as follows:

Q: Imagine that you used isoprene as diene – in that case you don’t have to worry about assigning endo…

A: When a conjugated diene and an alkene (dienophile) reacts to form an unsaturated six membered carbon…

Q: Draw the major organic product of the reaction shown below. K2Cr2O7 H2SO4, H₂O OH • You do not have…

A: Given that, the reaction is:

Q: Pd, NEt3, PPh3 CO₂Et

A: To write the product and mechanism of the given reaction:

Q: A) Draw the products of this reaction that agree with the product ratios at each temperature wher…

A: It is a [4 + 2] cycloaddition reaction between diene and dienophile, known as Diels-Alder reaction.…

Q: Indicate the increasing order of speed in an electrophilic aromatic substitution of a benzene that…

A: The objective of the question is to determine the increasing order of speed in an electrophilic…

Q: Show how to synthesize the target compound from the given sources. Hint: 1) a few steps are…

A: The Heck reaction is the reaction to form a substituted alkene from an unsaturated halide and an…

Q: Show the detalled, step-wise mechanism of the substitution reaction below and predict whether only…

A: One of the major class of organic reactions are substitution reaction. In substitution reaction, one…

Q: State whether it is possible to carry out each of the following nucleophilic substitution reactions.…

A: For nucleophilic substitutions reaction the reactant should have good leaving group and should be…

Q: You have learned two ways to make an alkyl benzene: Friedel–Craftsalkylation, and Friedel–Crafts…

A:

Q: One of the following Diels-Alder reactions will occur more rapidly than the other. Draw the major,…

A: The Diels-Alder reaction is a cycloaddition reaction between a conjugated diene and a dienophile…

Q: Using the attached molecule and synthesis, please redraw the molecule showing the stereochemistry…

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Q: 2) Provide a detailed mechanism for the addition reaction shown below. State the regiochemistry and…

A: The attack by the incoming group preferential at one centre over the other is known as…

Q: Pt(PPh,), catalyst

A: A step-wise mechanism for above reaction is attached below

Q: Q5) Which one of the following is(are) required for the Halogenation of aromatics? A] Catalyst B]…

A: Note: According to our guidelines we are supposed to answer only first three questions.  Kindly…

Q: Indane can undergo free-radical chlorination at any of the alkyl positions onthe aliphatic ring.…

A: The possible monochlorinated products from the given free-radical chlorination of indane are shown…

Q: Question: How do quantum mechanical effects influence the stability and reactivity of molecules with…

A: The question asks about the influence of quantum mechanical effects on the stability and reactivity…

Q: For which reaction mechanisms—SN1, SN2, E1, or E2—are each of thefollowing statement true? A…

A: The given reaction mechanisms are SN1, SN2, E1 and E2 To find: The mechanisms which involves…

Q: Which is/are true about SN1 mechanism? a) two-step reaction b) less substituted alkyl halyds react…

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Q: Write in full the mechanism for monobromination of cyclobutane. Be sure to include initiation, all…

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Q: carbocation

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Q: Consider the following incomplete photochemical pericyclic reaction. hu Draw the structure of the…

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Q: Optically active 2-butanol slowly racemizes on standing in dilute sulfuric acid. what type of…

A: Dilute H2SO4 on treating with optically active R-2-butanol, turns into a racemic mixture of 50%…

Q: WS-6.4: Draw the reaction mechanism for when 3-Bromo-3-methylpentane reacts with water. Next, draw…

A: A nucleophilic substitution reaction that occurs by an SN1  mechanism proceeds in two steps-1] In…

Q: Write mechanism for the free radical Bromination of ethylbenzene. Include all possible resonance…

A: Free radical bromination of ethyl benzene involves the formation of free radicals. The bromine is…

Q: Figure 1. Diels-Alder Reaction Between Anthracene and Maleic Anhydride AICI, or heat

A: the Diels-Alder reaction is a chemical reaction between a conjugated diene and a substituted alkene,…

Q: Predict the Mechanism which will inform stereo and regioselectivity on table given. Answer on…

A: The following mechanism and the bases and electrophile will be mentioned in a list given below. Also…

Q: V. In the following reaction: CH3CH₂Br + CH3COOK → CH3COOCH₂CH3 +KBr Adding a small amount of sodium…

A: SN2 reactions are nucleophilic substitution reactions which involve a backside attack by a…

Q: Outline an acceptable step by step mechanism for the Nucleophilic aromatic substitution of…

A: In an aromatic nucleophilic substitution reaction, at first, nucleophile reacts with aromatic…

Q: Among a primary, secondary, or tertiary carbocation, which is most favored for SN1 reactions?…

A: Among a primary, secondary or tertiary carbocation which is most favored for SN1 reactions? Explain…

Q: Write out the reactions for 2 - bromopentane undergoing BOTH substitution and elimination with…

A: Step 1: Step 2: Step 3: Step 4:

Q: Initiation: Propagation: Termination:

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Q: 5) If the reactant provided is neutral what can be done in basic conditions to produce a…

A: In a SN2 reaction a nucleophile attack the leaving group contaning Carbon and remove leaving group…

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.