Explain why each name is incorrect, and then write a correct name for the intended compound: (a) 2-Ethyl-1-propene The name is incorrect because the numbering of the chain is not correct V The correct IUPAC name is 2-methyl-1 butene (b) 5-Isopropylcyclohexene The name is incorrect because the parent name is not the longest chain V The correct IUPAC name is 4-isopropylcyclohexene (c) 4-Methyl-4-hexene The name is incorrect because The correct IUPAC name is (d) 2-sec-Butyl-1-butene V. The correct IUPAC name is The name is incorrect because (e) 6,6-Dimethylcyclohexene V. The correct IUPAC name is The name is incorrect because (f) 2-Ethyl-2-hexene The correct IUPAC name is A K7InternetSecurityEs K7InternetSecurityEssential: Click here to resolve.. The name is incorrect because

Explain why each name is incorrect, and then write a correct name for the intended compound: (a) 2-Ethyl-1-propene The name is incorrect because the numbering of the chain is not correct V The correct IUPAC name is 2-methyl-1 butene (b) 5-Isopropylcyclohexene The name is incorrect because the parent name is not the longest chain V The correct IUPAC name is 4-isopropylcyclohexene (c) 4-Methyl-4-hexene The name is incorrect because The correct IUPAC name is (d) 2-sec-Butyl-1-butene V. The correct IUPAC name is The name is incorrect because (e) 6,6-Dimethylcyclohexene V. The correct IUPAC name is The name is incorrect because (f) 2-Ethyl-2-hexene The correct IUPAC name is A K7InternetSecurityEs K7InternetSecurityEssential: Click here to resolve.. The name is incorrect because

Introductory Chemistry: A Foundation

9th Edition

ISBN:9781337399425

Author:Steven S. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Donald J. DeCoste

Chapter20: Organic Chemistry

Section: Chapter Questions

Problem 125AP

See similar textbooks

Similar questions

No explanantion or anything needed just draw the compounds in organic chem
Draw the structure of the given compound. Identify if the given name is correct of incorrect. If not, provide the correct IUPAC name of the compound. Don’t use CIS/TRANS or E/Z in naming the compounds. 1) 6-PROPYLCYCOHEPTENE 2) 7-BUTYNYLDODEC-1-ENE Note: need answers immediately. Will give a good rate right away as well.
Choose one of organic compounds (Eg: benzoic acid) that we always found in our daily life. State the source of the chosen compound and and give it's 3 benefits to us.
3..Name the IUPAC for the following compound.
Choose one of organic compounds that we always found in our daily life. State the source of the chosen compound and and give it's 3 benefits to us.
Referring to the named structures below, Choose:A if 1 st statement is true and the second statement is falseB if 1 st statement is false and the second statement is trueC if both statements are trueD if both statements are false 1. I: Structure A is an aromatic compoundII: Structue B is an alkane2. I: Structure C is not an aromatic compoundII: Strucure C and D are aliphatic hydrocarbon3. I: Structure F is not an aromatic hydrocarbonII: Only F is hydrocarbon4. I: Only Structure G will decolorize bromine solutionII: Structure H will produce brown solution upon basic oxidation5. I: Structure J will produce brown precipitate when potassium permanganate was addedII: Structure I will broduce yellow oil upon nitration6. I: Compound K is an aldehydeII: Compound L is an ketone7. I: Structure M is not an aldehydeII: Structure N is a ketone8. I: DNPH test cannot differentiate O and PII: Lucas test can differentiate O and P9. I: Compound Q will not react in Lucas testII: Compound R will react…
TRUE OR FALSE 1.The general reaction in alkene and alkyne is electrophilic substitution reaction. 2. Glycerin is also called a biological antifreeze 3. Octyne has a higher boiling point than Dodecyne 4. Alcohols that contain more than one hydroxyl groups taste bitter 5. Phenols are toxic to microorganisms that's why it is not advisable for it to be used as an antiseptic
1. Name of the following compound 2.Draw sec-butyl-tert-butylacetylene
Give IUPAC names for the following compounds: (attached pic)
in the structure, replace the "A" labels with groups to satisfy all of these conditions:- Put a Br anti to the methyl group already drawn in.- Put a hydroxyl group (OH) gauche to F and anti to Cl.- Put a benzene ring anti to F. (You will need to replace the "A" with a carbon when you do this.)
here's the reaction to be used for reference: C2H4 + H2 --> C2H6 1. What type of reaction is involved in C2H4 + H2 --> C2H6? 2. What is C2H4 in the reaction? 3. What is the name of the product in the reaction? a. ethane b. ethene c. ethyne
1. Draw the structure of 4-ethoxy-2,2-dimethyldecane. EXAMPLE Provided: