Explain the General Features of Radical Reactions ?

Q: All are true or false    a) A radical contains an atom that has an octet of electrons. b)…

A: Atoms react to attain stability. The reactivity is inversely proportional to stability. If the atom…

Q: Explain the Carbocation Rearrangements ?

A: Carbocation rearrangement is defined as the movement of a carbocation from an unstable state to a…

Q: (i) Write Reimer-Timann reaction.

A: When phenols are reacted with chloroform in the presence of sodium hydroxide, an aldehyde group…

Q: Draw three resonance forms for the cyclohexadienyl radical

A: We'll answer the first question since the exact one wasn't specified. Please submit question…

Q: Can you explain the process of free radical bromination by using methylcyclohexane?

A: This reaction have done in three step.  Step1: Chain Initiation Formation of two free radical Step2:…

Q: During sulphonation of benzene, H2SO4 generates the electrophile SO2 O "HSO4 O SO3 O +H O

A: In this question, we will Identify which electronphile is generated from sulphonation reaction on…

Q: What are the Possible Mechanisms for Nucleophilic Substitution ?

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

Q: The compound below is treated with chlorine in the presence of light. CH3CH2CH2CH3 Draw the…

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Q: Why is Ch3coo- a better nucleophile than OH-?

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Q: 9) CH,CH2CH=CH2 + HBr peroxides ( 10 )CH3CH,CH=CH2 + HBr ( 1 Br .CH3 1) ВН; THF 2) H2O2,OH (12)

A: We have to predict the product of the following given reactions as follows in step 2:

Q: Draw structure of Pyridine to show the orbitals involved in conjugation system

A: The structure of Pyridine to show the orbitals involved in conjugation system has to be drawn

Q: Differentiate an internal alkyne from terminal alkyne in terms with its reactivity with test…

A: Terminal alkyne have acidic proton due to which on reaction with an alcoholic solution of AgNO3 and…

Q: Nucleophilic substitution is a general reaction of organic compounds. Why, then, are alkyl halides…

A: SOLUTION: Step 1: Nucleophilic substitution reactions are a class of reactions in which an electron…

Q: explain why homolysis of the O-H bond in phenol requires considerably less energy than homolysis of…

A: a) O-H bond in phenol is more polar as compared to O-H bond in ethanol. This is because the…

Q: 2. progressive bromination of methane with the aid of sunlight

A: 1. This reaction proceeds in presence of light of photochemical conditions.  2. The reaction…

Q: Why is there a need to adjust the acid concentration of Group II cations before saturation with H2S?

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Q: Draw all resonance structures of the radical that results from abstraction of a hydrogen atom from…

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Q: Which carbon will most likely undergo radical halogenation when reacted with Br, in the presence of…

A: Note: As per our guidelines, we are supposed to answer only one question. Please repost the other…

Q: Whats the name of this structure using the systematic name of the alkyl radical

A: The given compound is a univalent alkyl radical. The valency of the carbon-2 is not satisfied.  This…

Q: Are terminal alkynes considered weak or strong acids? Explain why.

A: Welcome to bartleby !  Introduction :  We have to tell terminal alkynes are weak or strong acids .

Q: Using examples discuss the effect of charge and electronegativity on the strength of nucleophiles

A: Since nucleophiles are those substance which can donate there electron pair to the electrophile…

Q: a. How many monochlorination products can be obtained from the radical chlorination of…

A: a.

Q: Explain mechanism for Chlorination  ?

A: Introduction- The addition of chlorine to hydrocarbons (for both that is either aromatic or…

Q: what will be the type of interaction of ethane with bromine: a) radicals b) ionic c) nucleophilic d)…

A: Halogenation of Alkanes occurs when any alkane (ethane) reacts with bromine.

Q: Each step of the propagation portion of the reaction mechanism for free radical chlorination uses…

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Q: Define the General Features of Nucleophilic Substitution ?

A: In nucleophilic substitution, a nucleophile (a species with an unshared pair of electron) reacts…

Q: Draw additional resonance structures for each species.

A: a.  The given species is cyclopropenyl radical.The delocalization of bond, lone pair, or free…

Q: Explain Hydrogenation and Alkene Stability ?

A: Hydrogenation reactions are those reactions in which unsaturated hydrocarbons (alkenes) will undergo…

Q: Explain the Stability of Allylic Carbocations ?

A: Carbocations are positively charged, sp2 hybridized trigonal planer structures. They are electron…

Q: Explain the use of crown ethers in nucleophilic substitution reactions ?

A: Given Explain the use of crown ethers in nucleophilic substitution reactions ?

Q: Alkyl Halide Aldehyde/ Alkene ketone a. CH3I C. b.

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Q: What is the general format of a reagent for the reaction of an alkene or alkyne to count as…

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Q: by elimination of an HCl molecule from a chloro-2-propane molecule is obtained: a) C2H4 b) C3H6 c)…

A: The proposed reaction scheme is shown below including the chemical structure of substrate and…

Q: Explain the mechanism for halogenation of alkenes ?

A: Halogenation of alkenes take place via addition reaction. Markonikov's addition reaction takes place…

Q: Explain the characteristics of electrophilic addition of HX to alkenes ?

A: GIVEN: The determine the characteristics of electrophilic addition of HX to alkenes Explanation:…

Q: Markovnikov’s Rule is based on the formation of stable carbonium ion intermediate. stable radical…

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Q: Alkyl Halide Aldehyde/ Alkene ketone CH3I

A: Fill in the blanks with appropriate compounds via Wittig reaction.

Q: What are Allylic Carbocations ?

A: Carbocations are electrophiles (species that accepts electron pair in a reaction) that has a…

Q: Explain the importance of Pericyclic Reactions? Why should we study ?

A: Pericyclic reactions are defines as the reactions that occurs by concerted cyclic shift of electrons…

Q: Use the extended version of Markovnikov’s rule to predict the regiochemistry (orientation) of…

A: Addition of unsymmetrical alkenes In terms of reaction conditions and the factors affecting the rate…

Q: Explain Stability of Alkenes ?

A: A type of hydrocarbon that has carbon-carbon double bond in them is alkene. The general formula of…

Q: Enols are quite reactive toward electrophiles than alkenes because:

A: Enol is a common name for alkenol which is a group of structures consists of a double bond ( alkene)…

Q: Define nucleophilic aromatic substitution ?

A: Those reactions which involves replacement of one atom or a molecule of any one compound by another…

Q: This reaction is classified as: NCH3 CH3NH2 O A) Nucleophilic substitution B) Nucleophilic addition…

A: The answer is given as follows  Ans: nucleophilic addition

Q: Explain the Types of Pericyclic Reactions ?

A: A pericyclic reaction is an organic reaction where the transition state has cyclic geometry and the…

Q: Alkyl halide Aldehyde/ Alkene ketone b.

A: the reaction between a phosphonium ylide and an aldehyde or ketone to form an alkene is known as the…

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.