7- What are compounds I and II for the following reaction? Benzaldehyde + [Ag(NH3)2]NO3 → I+ 2Ag(s) I + acidified methyl alcohol ->>> > II A. I: Acetophenone, II: Ketal B. I: Benzoic acid, II: Hemiacetal C. I: Nitrobenzene, II: Methyl benzoate D. I: Benzoic acid, II: Methyl benzoate 8- An aldehyde group can be present A. only at the end of carbon chain B. at the second carbon atom of the carbon chain C. at any position in carbon atom D. in between carbon chain 9- What is the structural formula for acetophenone? CH3 A. B. C. D. CH₂ CH,

7- What are compounds I and II for the following reaction? Benzaldehyde + [Ag(NH3)2]NO3 → I+ 2Ag(s) I + acidified methyl alcohol ->>> > II A. I: Acetophenone, II: Ketal B. I: Benzoic acid, II: Hemiacetal C. I: Nitrobenzene, II: Methyl benzoate D. I: Benzoic acid, II: Methyl benzoate 8- An aldehyde group can be present A. only at the end of carbon chain B. at the second carbon atom of the carbon chain C. at any position in carbon atom D. in between carbon chain 9- What is the structural formula for acetophenone? CH3 A. B. C. D. CH₂ CH,

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter8: Alkenes: Reactions And Synthesis

Section8.SE: Something Extra

Problem 37MP: Dichlorocarbene can be generated by heating sodium trichloroacetate. Propose a mechanism for the...

See similar textbooks

Similar questions

The methoxy group is reported as having σpara and σmeta values that differ in sign (σmeta =+0.12; σpara = –0.27). What specific experiments are performed to determine these s values?Explain why the σpara and σmeta values are of different sign and what those signs indicate.
Prove that the Keq for the reaction between Pb2+ and HF is 12.4. (Ksp, PbF2 = 6.76 x 10-4 and dissociation constant of HF is 3.7 x 10-8)
Predict the product of the following reaction and classify the reaction. Pb(NO3)2+FeSO4--->PbSO4+________
the dissociation constant of 0.25 M propanoic acid C2H5COOH is 1.3 × 10-⁵. a) What is the dissociation rate of C2H5COOH in this solution?
In light of your answer to Problem 30-40, explain why a mixture of products occurs in the following reaction:
Dichlorocarbene can be generated by heating sodium trichloroacetate. Propose a mechanism for the reaction, and use curved arrows to indicate the movement of electrons in each step. What relationship does your mechanism bear to the base-induced elimination of HC1 from chloroform?
Provide the mechanism and products for the acid-catalyzed epoxide opening reactions below, including appropriate stereochemistry.
The nitroso group, −N=O, is one of the few nonhalogens that is an ortho- and para-directing deactivator. Explain this behaviour by drawing resonance structures of the carbocation intermediates in ortho, meta, and para electrophilic reaction onnitrosobenzene, C6H5−N=O.
please provide the mechanisims for the reactions of 1a ,1e,1f
6. Identify the best reagent(s) for this reaction. (see attached screenshot). a. H2SO4, HgSO4, H2O b. 1. Disiamylborane, 2. HO–, H2O2 c. K2Cr2O7, H+ d. NaOCl e. H2, Pd
I’m currently trying to write a lab report for the synthesis of dimolybdenum tetraacetate [Mo2(O2CCH3)4] from the reaction of molybdenum hexacarbonyl, Mo(CO)6 in glacial acetic acid and acetic anhydride under a nitrogen atmosphere, involving the difficult formation of a quadruple bond and requires high heat and long reaction time (approximately 20 hours). But these are the question I’m stumped on: 1. Why need the reaction be done under nitrogen? We also added dichlorobenzene and hexanes during the reaction. 2. Explain the purpose of dichlorobenzene and hexanes. 3. Why does the reaction take 20 hrs?
Which one of the following reagents is capable of transforming Fe2+(1 M) to Fe3+(1 M)? Br-(1 M) H2 (1 atm) H+ (1 M) Br2