Concept explainers
Interpretation:
It is to be verified whether the nitrile in the given reaction is reduced by calculating the oxidation state of the carbon and the nitrogen atoms of the
Concept introduction:
The oxidation state of an atom can be calculated using two steps.
First is to assign the proper number of valence electrons to the atom. In this case, both electrons of a lone pair are assigned to the atom on which they appear. In a covalent bond, all the electrons are assigned to the more electronegative atom. If the two bonded atoms are the same or have comparable electro-negativities, then electrons get divided equally to both the atoms.
Second is by comparing the assigned valence electrons to an atom to the
In general, the loss of electrons from the reactant side to the product side is termed as oxidation while the gain of electrons is termed as reduction.
Want to see the full answer?
Check out a sample textbook solutionChapter 17 Solutions
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
- I need help on this question, please!arrow_forwardPlease don't provide handwritten solution.....arrow_forwardPlease answer this Can you give examples to explain Addition reactions-general characteristics Benzene rings do not reactthi like alkenes Remember, the electrophile adds to the less substituted carbon, and the nucleophile to the more substituted carbon. Markovnikov’s Rule: The addition of a hydrogen halide to an alkene favors the product in which the proton adds to the alkene carbon that is initially bonded to the greater number of hydrogen atoms. Carbocation rearrangements- Methyl groups and hydride groups can migrate to make a more stable carbocation. A primary carbocation is less stable than a secondary carbocation, which is less stable than a tertiary carbocation. Addition of A Strong Bronsted Acid Hydrohalogenation HX addition to an alkene. Goes through a carbocation intermediate. The electrophile (H+) adds to the less substituted carbon, and the carbocation forms on the more substituted carbon. The nucleophile (X-) then adds to the more substituted carbocation.…arrow_forward
- A benzene ring alters the reactivity of a neighboring group in the so-called “benzylic” position, similarly to how a double bond alters the reactivity of groups in the “allylic” position. Benzylic cations, anions, and radicals are all more stable than simple alkyl intermediates. a) Use resonance structures to show the delocalization of the positive charge, negative charge, and unpaired electron of the benzyl cation, anion, and radical.arrow_forwardBe sure to answer all parts. By taking into account electronegativity differences, draw the products formed by heterolysis of the carbon-heteroatom bond in the following molecule. Classify the organic reactive intermediate as a carbocation or a carbanion. Use a skeletal structure to draw the organic ion. Li draw structure .arrow_forwardClassify your he following substituents according to whether they are electron donors or electron accepters relative to hydrogen by the resonance and the inductive mechanisms a= acceptor D=donor n= no effect please double check and see everything is correct I had submitted this question multiple times and gotten it incorrect I have no more ask questions left to send.arrow_forward
- ← Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the intermediate and the final product formed in this reaction. Include all lone pairs and charges as appropriate. Ignore inorganic byproducts. Problem 382 of 2 ེ་ ཆོས་རིག་ཆ་ Draw Intermediate 0° Darrow_forwardskip this if you already this. typewritten or handwritten but readable. if I it is not readable I will downvote. If I see the same answers I will downvote.arrow_forwardFor the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H2SO4H2SO4, then draw the structures of the minor and major products of the elimination.arrow_forward
- Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to draw the intermediate and product of this reaction or mechanistic step(s). Include all lone pairs and charges as appropriate. Use wedges and dashes to indicate stereochemistry. Ignore inorganic byproducts.arrow_forwardCurved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to draw the intermediate and product of this reaction or mechanistic step(s). Include all lone pairs and charges as appropriate. Use wedges and dashes to indicate stereochemistry. Ignore inorganic byproducts.arrow_forwardIn the following acid-base reactions, 1. draw Lewis structures of the reactants and the products. 2. determine which species are acting as electrophiles (acids) and which are acting as nucleophiles (bases). 3. use the curved-arrow formalism to show the movement of electron pairs in these reactions, as well as the imaginary movement in the resonance hybrids of the products. 4. indicate which reactions are best termed Brønsted-Lowry acid-base reactions. (c) -BH₁₂ BH3 + CH3-O-CH3 → CH3-O-CH3 (d) 유 0- CH3-C H + -OH CH₁₂-C-H OHarrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning