Question

400 Name: / 25 1. Write the names for the compounds. (8 pts) CH,CH2CH2CH2CH,COH сн,сн,а сн,сна CH3CH2CH COCH,CHE 1-CH₂ CH₃ о
0 0
Add a comment Improve this question Transcribed image text
Answer #1

The answer of the following questions are given below;

d-on 2. да си си, си,си, сH, - - 6 5 4 3 hexanos cacict IUPAC NAME ен, си,си, - c-oc, M Ethyl-butanoate. IUPAL Nomenclatwa دا

Add a comment
Know the answer?
Add Answer to:
400 Name: / 25 1. Write the names for the compounds. (8 pts) CH,CH2CH2CH2CH,COH сн,сн,а сн,сна...
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
  • (48 pts, 4 pts each) Give an acceptable IUPAC name for the following compounds 1. CH b. coH CH C. OH DO d. ollal ol...

    (48 pts, 4 pts each) Give an acceptable IUPAC name for the following compounds 1. CH b. coH CH C. OH DO d. ollal ol oun COOH е. Br f. CH2 Br CH-CH,-CH-CH2-CH- CH,-CN

  • 1. Give the IUPAC systematic names for the compounds drawn below. my H2C hongiran wa y...

    1. Give the IUPAC systematic names for the compounds drawn below. my H2C hongiran wa y they This is a free to the tutorial forces will start their restit This moterial is continet and it to Thiru vana Turner will not Continued from previous page нс H-C сн mag me on you нсо OCH не х", сн, F3CCF 2. Using reactions that we have covered this semester, give SIX different ways to make a carboxylic acid that each start from...

  • 1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c)...

    1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c) ОН ОН (d) Br ОН ОН NH2 2) Draw the condensed and line structures for the following compounds (a) 3,4-dimethylhexanoic acid (b) Phenylacetic acid (c) 3,4-dinitrobenzoic acid (d) 2,2,3-triflurobutanoic acid (e) 3-hydroxybutanoic acid (1) o-hydroxybenzoic acid (g) a-aminopropionic acid 3) Name the following dicarboxylic acids (use both IUPAC and common names) Он (а) НО ОН НО. (b) он ОН ОН (d) ОН он ОН...

  • 1 An alkyne with the formula CaHe (8 pts) ODranw the folowing compounds Mofa isoproply Acetone...

    1 An alkyne with the formula CaHe (8 pts) ODranw the folowing compounds Mofa isoproply Acetone tions and and the conditions a 2 (8 pts) Provide the MAJOR product for the folowing reactions. The starting material the type of reaction are all given Starting Material Reactants HYDRATION catalytic H and HOH A) DEHYDRATION H' and heat> Acid Base ReactionC) NaOH Acid Base Reaction D) HCI 3.(4 pts) Circle any chiral carbon(s) in the following structures of anesthetics or write NONE...

  • Name Chem 110 Oct 15, 2019 Write the formulas from the names of compounds 1. sulfur...

    Name Chem 110 Oct 15, 2019 Write the formulas from the names of compounds 1. sulfur dioxide 2. manganese (IV) oxide 3. sodium thiocyanate N aSON 4. lithium phosphate 5. nickel (II) nitrate Ni (NO2)2 6. ammonium chloride 7. potassium chlorate ka 8. beryllium periodate 9. cadmium chromate Cd Croa 10. sodium permanganate 11. iron (II) hydroxide Fe(OH)2 12. trinitrogen pentoxide 13. strontium nitride SraN₂ 14. magnesium bromate 15. sodium thiosulfate Na.S.O. 16. chlorous acid 17. sodium hypobromite Brno 18....

  • extra credit orgo chem NaBH MOH 1.Write two starting materials (five or fewer C's) that react...

    extra credit orgo chem NaBH MOH 1.Write two starting materials (five or fewer C's) that react to form the target molecule starting from any carbonyl compound and any organometallic reagent. OH Part IV. Mechanistic Puzzlers (16 pts) 10. Reduction of cyclohexanone using lithium aluminum hydride gives a deuterated alcohol when D.O is used instead of H.O in the workup step. Account for this outcome with a mechanism, showing curved arrows, the key intermediate, and lone pairs and charges. (6 pts)...

  • 6. Provide the IUPAC names for the compounds below Name: 7. Draw the following: cis-1-isobutyl-2-propyleyclopentane 8....

    6. Provide the IUPAC names for the compounds below Name: 7. Draw the following: cis-1-isobutyl-2-propyleyclopentane 8. Label the indicated atoms in the structure below as 1º, 2º, 3º, or 4º. PB A A B co 9. Draw Newman projections for the day-diethylane about the C4CS bond, Circle the most stable conforme if you need additional space, please feel free to the backside of this paper 10. Draw the chair conformation and ring-flip for the given compound. Calculate the sterie strain...

  • 26) Name the following compound. CH3 H2C=CH-CH2CHCH: A) 1,1-dimethyl-3-butane B) 4-methyl-1-pentene C) hexene D) 2-methyl-4-pentene E)...

    26) Name the following compound. CH3 H2C=CH-CH2CHCH: A) 1,1-dimethyl-3-butane B) 4-methyl-1-pentene C) hexene D) 2-methyl-4-pentene E) 2-methylpentene 27) Name the following compound. CI A) 2,3,5-trichlorobenzene B) trichlorostyrene C) 1,3,4-trichlorobenzene D) 1,3,4-trichlorohexene E) 1,2,4-trichlorobenzene 28) Identify the formula for an alkene. A) CnH2n+4 B) CnH2n+2 C) CnH2n D) CnH2n-4 E) CnH2n-2 29) Name the following compound. A) 1,4-bromocyclohexene B) 1,4-dibromobenzene C) 3,6-dibromobenzene D) 2,5-dibromobenzene E) 2,5-dibromocyclohexene 30) Name the following compound. CECH CH,CH,CHCH A) 2-ethynebutane B) 3-methyl-1-pentyne C) 3-methyl-4-pentyne D) 3-ethyl-1-butyne...

  • ____ 1. The diagram below represents serine, a polar, uncharged amino acid. Which functional group gives...

    ____ 1. The diagram below represents serine, a polar, uncharged amino acid. Which functional group gives serine its distinct property? a. H3 b. CH2OH c. –H d. COO– ____ 2. The monomers shown below are monomers for which of the following natural polymers? a. polysaccharides b. plastics c. DNA d. proteins ____ 3. Which of the following processes illustrates the production of a protein? a. specific code for amino acids --> amino acid chain --> gene --> DNA --> specific...

  • 1) Write a Reaction equation using 4- aminobenzenesulfulfonic acid (aniline derivative) and 8-ani...

    1) Write a Reaction equation using 4- aminobenzenesulfulfonic acid (aniline derivative) and 8-anilino-1-naphthalenesulfonic acid (coupling agent). Write the mechanism. SYNTHESIS OF AZO DYES INTRODUCTION Humans' love of color dates back almost to prehistoric times, yet it is not actually until the modern era that the full range of the rainbow has been accessible to the majority of people irn their clothes and other textiles. Ancient or medieval times have often been described as being quite splendid with their "tyrian purple"...

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