Concept explainers
(a)
Interpretation: The carbon radical which is formed by homolysis of the
Concept introduction: The formation of carbocation, carbanion and free radical occur due to the heterolysis or homolysis process. Homolysis is opposite to the heterolysis. It forms radical with an unpaired electron.
Resonance is the delocalisation of
(b)
Interpretation: The carbon radical which is formed by homolysis of the
Concept introduction: The formation of carbocation, carbanion and free radical occur due to the heterolysis or homolysis process. Homolysis is opposite to the heterolysis. It forms radical with an unpaired electron.
Resonance is the delocalisation of
(c)
Interpretation: The weaker
Concept introduction: The energy which is released or absorbed in the
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- Consider the SN2 reaction below. NaN3 N3 DMSO Sodium azide (Na+ N3) is the nucleophile in this reaction. a. Draw a Lewis structure for the azide anion (N3). Be sure to show ALL formal charges. b. Provide a resonance form for the azide anion. Show electron movement using curved arrows. C. Which these structures (a or b) is the highest resonance contributor? d. What will be the effect on the rate of the reaction if [NaN3] is tripled? Circle one response. The reaction rate: a. doubles b. triples c. quadruples d. remains the same e. none of the above page 8 of 17arrow_forwardPart IV: Draw the mechanism and the energy diagram for the reaction shown below. Include any resonance structures for the intermediates of the reaction. Br A OHarrow_forwardWhy does bromination reactions occur only on more stable radicals? O a. Br₂ is less reactive than Cl₂. O b. Br₂ is more reactive than Cl₂. O c. Br₂ is less selective than Cl₂. O d. Both a and c.arrow_forward
- 4. A student wants to make molecule B with the following reaction below. Instead of molecule B, a different molecule is made. Give the structure of this compound. HO HO OH H₂NOH * HO N OH HO B OHarrow_forward40arrow_forwardConsider the following structures: CH, CH3 H;C, „NH3 H,C, CH H3C, Br H3C. CH CH3 CH3 CH3 JECE CEEJ JEEC СЕЈЕ ЕСЕ Which is a resonance contributor? ECJE Which has a net formal charge of +1? JECE Which has only one type of hydrogen? ECJE Which will form the most stable free radical? JEEC Which is an electrophile? JEECarrow_forward
- Draw the least stable resonance form for the intermediate in the following electrophilic substitution reaction.arrow_forwardN,N-diethyl-m-toluamide (DEET) is the active ingredient in many insect repellent preparations. Following is one of the steps in its synthesis. In the box below draw the structure of the product of this reaction. H3C MgBr 1. CO2 2. H3O+ product • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • Draw the Grignard reagent as a covalent magnesium bromide. 90-87 0 + 11 ? n [arrow_forwardWhich statement about elimination reactions is true? Two σ bonds are formed. Two π bonds are broken. Two π bonds are formed. Two σ bonds are broken.arrow_forward
- This is a Bransted-Lowry acid-base reaction. Draw structures for all the products, showing any non-zero formal charges in each one. Make sure your reaction is balanced. Note for advanced students: Draw only the most stable resonance structure for each product. NH,—CH,–CH=CH, + KOH 11 Click and drag to start drawing a structure.arrow_forward1. What is the bond angle in carbon tetrachloride? 2. What is the product of the reaction of pent-2-ene with Cl2? 3.Which statement is correct? * A. The bond length increases when the difference between the electronegativity of the atoms is higher B. The bond length increases when the number when there is an increase in pi bonds. C. Increasing the bond polarity increases the bond length. D. Sp2 has shorter bond length that sp. 4. How many moles of O2 gas is theoretically needed for 1 mole of hexane? 5. What is the MOST LIKELY product of the reaction of pent-1-ene with HCL? 6. Which one creates a sigma bond? * A. 2 pz atomic orbitals B. 2 py atomic orbitals C. 2 px atomic orbitals D. none of these 7.How many hydrogen atoms are there in trans-1-bromo-2-methylcyclohexane? 8.arrow_forwardPayalbenarrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning