Name these compounds using IUPAC rules.
Name these compounds using IUPAC rules. Name these compounds using IUPAC rules. (20 points; 5 each)...
1. Name these compounds using IUPAC rules. (20 points; 5 each) COCH3
20. (10 points) Name or draw a structure for each of the following molecules using IUPAC rules. CH2CH2CH3 HỌC=CHC(CH3)2CH CHỊCH, C=C HH
Total L (15 points, 5 points each) Name (using IUPAC rules) or draw a. 3,3,8-trimethyl-5-(1-methylethyl)decane b. (2R, 3s)-2,3-dibromohexane (use Fischer projections please)
Using IUPAC rules, name the following organic compounds A. Br ОН B. C. ОН D, H E.
Give the IUPAC rules to name a byciclo with one branch Give the IUPAC rules to name compounds with functional groups and with branches (same as 3) just the double bond changes for functional group. The double bond is a functional group. Give the names of the branches that have common names. Those names are now accepted by IUPAC since they are here to stay. e.g isopropyl Give the name of the branches in 6 using IUPAC nomenclature. e.g isopropyl...
Using IUPAC rules, name the following organic compounds F. G. I. COOH J w
Using IUPAC rules, name the following 6 organic compounds. I will rate quickly once answered! A. COOH B. C. HO Br om muk innt E.
3. Name each of the following compounds using IUPAC nomenclature, including stereochemistry if applicable. (18 points) Br, I "I н "Br
Please answer all parts for good rating! A) Name the following compounds using IUPAC rules: B) Provide the structures for the compounds below: 4-bromobutanal acetophenone yy fty For the following reaction, provide the structure of the open- chain form of the compound (pay attention to stereochemistry) and the complete arrow-pushing mechanism for the reaction. open-chain form HO Starting with the compound shown and only alcohols (including diols) of three carbons or less, suggest a means by which to achieve the...
5. Nomenclature (16 points). a. Give the IUPAC name of each of the following compounds НАС H3C b. Draw structures for the following compounds. 5-ethyl-5-iododecane 2,4,6-trichloroheptane Three structural (constitutional) isomers of bromochloropropane