siame. hswers on the answe I. Multiple Choice: Chose the on 1. Which one of the following dienes will not react in a Diels Afder reaction? of C 2. Which one of the following compounds will not react by Friedel-Crafts alkylation or acylation? -NHCH3 CH3 -NHCHO C ich one is the anti-aromatic compound?

siame. hswers on the answe I. Multiple Choice: Chose the on 1. Which one of the following dienes will not react in a Diels Afder reaction? of C 2. Which one of the following compounds will not react by Friedel-Crafts alkylation or acylation? -NHCH3 CH3 -NHCHO C ich one is the anti-aromatic compound?

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Part 1 Choose the protecting group to use in the first step: Choose one: O 1e0 HOCH2CH:OH, H:O- O H20, H3O- O 1ec DHP, H:O a 1sc H2C=0, H:O- O H20, N3OH Please show wechanisms, . Part 2 choose 1. LIAIH, 2. H;O' protecting group product Draw the final produc: (after the protecting group has been removed):
Choose the correct starting material and reagents for this transformation using a Diekmann cyclization reaction. conditions A OEt 541 H3C CH3 1. NaOEt, EtOH OEt 2. H3O+ 1. NaOEt, EtOH 2. H3O+ 1. NaOEt, EtOH 2. H3O+ The following reaction scheme: Br H3C CH3 The following reaction scheme: EtO The following reaction scheme: EtO H3C CH3 The following reaction scheme O HỌC CH. H3C CH₂O O OEt OEt 1. NaOEt, EtOH 2. 요
Fill in the table below indicating what is important in each category for an SN1 reaction and an SN2 reaction. SN1 Rate Law Best Solvent Stereochemical outcome How does substitution on electrophile affection the reaction? Does leaving group ability affect the rate? Does nucleophile strength affect the rate? What types of nucleophiles are best? SN2
8:00 Problem 29 of 40 conc. HBr SOS 63 ..... Draw the products of the two step reaction sequence shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore inorganic byproducts. H₂O Done
Explain the observed reactivity rate of the following alkyl halides in an SN1 reaction. -CI slowest rate anti-aromatic least stable answer. + non-aromatic CI CN Propose the product of the following reaction (hint: this is a two step-reaction. Reaction one is an electrocyclic ring opening and step 2 is a cycloaddition reaction). Be sure to include stereochem in your CN fastest rate A CI aromatic most stable
Match the following with proper product or reagent Match each item to a choice: Halogenation of aikyne radical halogenation of alkene intermediate of oxidative cleavage Formation of acetylide from alkynes intermediate of diol formation Formation of trans- alkene from the alkyne Choices # NABH4 # L NH3 # osmate # molozonide # bromonium i peroxy acid # tetrahalide # vicinal dihalide # Hy, Lindlar catalyst
Complete this concept map to summarize all epoxide reactions: CH3 CH₂ НО. Weak Nuc, H₂O+ CH3 H3C 1. Strong Nuc 2. H₂O* NaOH H₂O
2. Draw the product and the mechanism of the following Diels-Alder reaction. میمی که Diels-Alder 3. How would you synthesize the following product from propylbenzene, using any other reagents necessary? NO₂
What is the major product of the following reactions? NaOCH3 ? а. O b. none of the other answers C. d. е.
19. Predict the major product for the following reaction. 22. Predict the major product for the following Diels-Alder reaction.
Between [i] and [ii], which structure is most likely to give a stable product? (i] H3C- -H- [ii] H3CO-H A. [i] and [ii] В. [i] C. [i] D. Both of this structures will not give stable products.
Design a three-step synthesis for the following conversion using a Diels-Alder cycloaddition reaction. Disregard stereochemistry and competing products. s-dr Part: 0/4 Part 1 of 4 CN CN A- CH3 CH₂ Draw the retrosynthetic dienophile precursor to the target molecule. Disregard stereochemistry and competing products. B +