Question
please answer d e f g
For each of the following structures: (a) Give the IUPAC name. (b) Identify the leaving group. (c) Identify the degree of sub
0 0
Add a comment Improve this question Transcribed image text
Answer #1

- BP a) IUPAC name A Azi on 1-Bromo butone longest carbonchain find then numbering Start with when -Br-attached. I b) Here on4. C! : (15,2R)-cid-chloro-2-methylcyclohexane Two groups are in up so eis. chloro and methyl substi thents bute commes first alphabatically Stost with-el. so numbering b) M e Here dis the leaving Group C) 2° Carbon where leaving groupe) Secondary Carbon d) . a. dil H4 Bre a) saHA 3 32 L3 » Here lowest Priority group in up so, s.LUL (15,35)-1-bromo-1,3-dimethyl cyclohexane b) - Br is the leaving Group e) teptiapy carbon (degree of substitution)

Add a comment
Know the answer?
Add Answer to:
please answer d e f g For each of the following structures: (a) Give the IUPAC...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • For each of the following structures: (a) Give the IUPAC name. (b) Identify the leaving group....

    For each of the following structures: (a) Give the IUPAC name. (b) Identify the leaving group. (c) Identify the degree of substitution of the carbon bearing the leaving group. (d) Identify the same carbon as (R) or (S), if applicable. (e) Give the product(s), if any of reaction with NaOH and with NaOCH3. (1) Identify the same carbon as in (c) and (d) in the product as (R) or (S), if applicable. (g) Choose the most appropriate solvent to facilitate...

  • please answer question For each of the following structures (a) Give the IUPAC name (b) Identify...

    please answer question For each of the following structures (a) Give the IUPAC name (b) Identify the leaving group (c) Identify the degree of substitution of the carbon bearing the leaving group. (d) Identify the same carbon as (R) or (S), if applicable. (e) Give the product(s), if any of reaction with NaOH and with NaOCH3 (f) Identify the same carbon as in (e) and (d) in the product as (R) or (S), if applicable (g) Choose the most appropriate...

  • 1.) Please name the following ketones and aldehydes "I that "mi 2.) Please give the product...

    1.) Please name the following ketones and aldehydes "I that "mi 2.) Please give the product of the following reactions NAH, CH OH (solvent) LiAIH Diethyl ether (solvent) 3.) Please give the product of the following reaction: ON "Dina NHANH (p-nitrophenylhydrazine)

  • 1. Write the predicted product and the rate law for the following reaction: CH;CH CH CI...

    1. Write the predicted product and the rate law for the following reaction: CH;CH CH CI + NaCN DMSO 2. In the following reaction, identify a) the leaving group, b) the nucleophile, c) the electrophilic carbon and d) the solvent CH CH Br + NaHS H30 CH CH SH + NaBr 3. Write out the reaction of (R)-2-bromopentane with sodium cyanide in DMSO, including the predicted major product: 4. Rank the following in decreasing order of leaving group ability (with...

  • Choose the best answer for the main type of reaction shown below: For an SN2 reaction, the BEST scenario would be: Selec...

    Choose the best answer for the main type of reaction shown below: For an SN2 reaction, the BEST scenario would be: Select the term that best identifies relationship between the two molecules shown. Choose the best answer for the main type of reaction shown below: (1 mark) EtOH a) b) 2° alkylhalide, Syl reaction, one product 2° haloalkane, Syl reaction, racemic products 2º haloalkane, Sn1/E1 reactions, racemic products and alkene products 2º haloalkane, Sn2 reaction, one product 2° alkylhalide, Sn2...

  • please explain!! 3 e) Which solvent is a polar protic solvent? a) ether c) ethanol b)...

    please explain!! 3 e) Which solvent is a polar protic solvent? a) ether c) ethanol b) dimethylformamide d) hexane Circle the correct name for the molecule shown below. Br (trans)-3-bromo-4-methyl-4-heptene (E3-bromo-4-methyl-3-heptene (Z)3-bromo-4-methyl-3-heptene (cis)-3-bromo-4-methyl-3-heptene g) Circle the reaction that would have the fastest rate. NaSH DMF SH NaOH OH B DMF NaSH DMF Br SH NaOH Br он DMF h) Circle the strongest nucleophile in methanol (CH,OH) F Br

  • [Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl...

    [Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl groups are isopropyl, isobutyl, sec-butyl, and tert-butyl. CH2CH3 CH3CH2CH2CCH2CH3 Submit Answer Retry Entire Group 9 more group attempts remaining The two reactants shown below are combined to bring about a nucleophilic substitution reaction. Br NaOCCH, . CH3CH2CHCH 1. none h. HBr 1.H20 e. "CCH3 f. Br j. Nat 9. HOCCH3 k. "OCCH3 Which letter designates the electrophilic carbon at which substitution occurs? (If no...

  • please help solve question 21 and question 22. thank you THE FOLLOWING REACTION SCHEME APPLIES TO...

    please help solve question 21 and question 22. thank you THE FOLLOWING REACTION SCHEME APPLIES TO QUESTIONS 21 AND 22 Jon + intos xor (2) Har Xothon QUESTION 21 [2] In the products of reaction (1), the halogen is on the less hindered carbon labelled (b) in the ether, and the oxygen remains on the more hindered carbon labelled (a). The reason for this is: 11 The reaction proceeds via an 2 mechanism, oxygen in the ether gets protonated first,...

  • Predict the major product(s) expected given the reagents shown below. Answer the following questions and use...

    Predict the major product(s) expected given the reagents shown below. Answer the following questions and use the answer so identify the likely mechanists pathway(s) (e.g., E2 or E1eB) Be sure to include the answers to the questions! What is the electrophile for this reaction? (Mark it with an*) Is the electrophilie carbon primary, secondary, tertiary, Is the leaving group excellent okay, or poor? (eg Good LG) Is the considered to be strong or weak? (e.g Strong Nu) Can the nueleophile...

  • Help with part e please! 3. Consider the following Sw1 reaction. CHg CH,-Ẻ-CHCH + HO ---...

    Help with part e please! 3. Consider the following Sw1 reaction. CHg CH,-Ẻ-CHCH + HO --- ne bo pomem e no — a potom os CHE CH-C-CHÚCH + I" OH a. Draw a mechanism for this reaction using curved arrows. b. Draw an energy diagram. Label the axes, starting material, product, E, and . Assume that the starting material and product are equal in energy. c. Draw the structure of any transition states. d. What is the rate equation for...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT