Analyze the reactant(s) and reaction conditions, then predict the structure of the major organic product and indicate the predominant mechanism (SN l, SN2, EI, or E2) of cach reaction.
Q: to Cl, + HCl A.
A: See answer below.
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A: Types of mechanism Nature of alkyl halides.
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Q: LOH HO Toluene, A 5-10 min °CO2H
A: This reaction is basically [4+2]-cycloaddition reaction occurs in presence of heat.
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A: In this reaction the amide group is converted into nitrile group by the following mechanism-
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A: Hey, since there are multiple questions posted, we will answer first question. If you want any…
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A: a)
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A: Interpretation- To propose a chain reaction mechanism for given halogenation reaction.
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Q: NaoCHy CH, ON A
A:
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A: Given Give the organic chemical reaction mechanism of the synthesis of 1-bromobutane.
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Q: Br H20
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A: The reaction is as follows:
Q: How many steps in the mechanism of this reaction?
A: Number of steps in the mechanism of given reaction = ?
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A: The details solution for this is provided below in attach image.
Q: action. cooH To Itoo ć cood
A: Decarboxylation reaction takes place
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A: Ans A
Q: Question attached
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- Following is an equation for iodination of toluene. This reaction does not take place. All that happens under experimental conditions for the formation of radicals is initiation to form iodine radicals, I , followed by termination to reform I2. How do you account for these observations?Trichloroisocyanuric acid, TCICA, also known as “swimming pool chlorine,” is a stable solid that oxidizes alcohols, following a mechanism similar to oxidation by HOCl. No reaction occurs between TCICA and the alcohol (in a solvent such as acetonitrile) until one drop of HCl(aq) is added, whereupon the reaction is over in a few minutes. Write the mechanism for this oxidation that shows the key role of the acid catalyst. Show the oxidation of just one alcohol, not three.Molecule: 6-chloro-4-ethylhex-2-enoic acid For the mechanism you will focus on the reaction of the portion of the molecule drawn only (not the R part). For any corrections, disregard the parts of your molecule represented by R-groups. Below the incorrect mechanism write a discussion (step-by-step) of the incorrect mechanism identifying all of the mistakes in the mechanism. Keep in mind that there will be more than one mistake in the given mechanism and that the product given is not necessarily the correct product of the reaction of your molecule with the given reagent. For each mistake, give a detailed, scientific explanation of why it is incorrect. Draw your own correct mechanism on a new page
- ORGANIC CHEMISTRY - PERICYCLIC REACTIONS Indicate the products, no need to design the mechanisms.Assign these reactions as SN1, SN2, E1 and E2 on the blank line on the right side of the reactionsAdd these 2 equations and obtain an overall reaction (cancel out compounds that appear in the reactants of one equation and the products of the other euaqtion and vice versa producing an overall equation reaction) (CH3)2SiCl2 +2H2O ----> (CH3)2Si(OH)2 +2HCl n(CH3)2Si(OH)2 -------->[(CH3)2SiO]n + nH2O
- C3H6 + H2O + H2SO4 --> C3H8O + H2SO4 what is the catalyst in the reaction above?Predict the products and mechanisms of the following reactions. When more than oneproduct or mechanism is possible, explain which are most likely. 2-chloro-2-methylbutane + NaOCH2CH3 in ethanolWrite the products A, B, C, D, E, F, G, H, I, J and K in the following reactions.
- Predict the products and mechanisms of the following reactions. When more than oneproduct or mechanism is possible, explain which are most likely. ) 1@bromo@1@methylcyclopentane + NaOEt in ethanolAre there any other possible products for the following reaction in catalytic H2SO4 and H2O?This is the type of organic reaction wherein a single reactant splits into two products and is accompanied by the formation of a small molecule. addition substitution elimination condensation What is the name of the angle that a nucleophile approaches the carbon on the C=O bond? Borge-Dante Bürgi–Dunitz Baran-Daly Bunsen-Debye