(3 pts) Provide 2 acceptable names for the molecule below. If you provide a systematic name,...
Trying to make sure my answer is right. Please explain if not! Thanks! 1. (3 pts) Provide 2 acceptable names for the molecule below. If you provide a systematic name, include the appropriate R or S designation in the name. 3-bromopropane Br 92-bromoprapy 2. (2 pts) Provide a systematic name for the molecule below. 12-dethy-dlaro heiane . (2 pts) Indicate whether the listed solvent is protic or aprotic. a. tert-butanol [(CH3)3COH] Protic protic b. formamide [HCON H2]
1. (3 pts) Provide 2 acceptable names for the molecule below. If you provide a systematic name, include the appropriate R or S designation in the name.
Write an acceptable IUPAC name for the compound below. (Only systematic names, not common names are accepted by this question.) Keep the information page open for feedback reference. The IUPAC name is Submit Answer Retry Entire Group 3 more group attempts remaining Write an acceptable IUPAC name for the compound below. (Only systematic names, not common names are accepted by this question.) Keep the information page open for feedback reference. The IUPAC name is Submit Answer Retry Entire Group 3...
Write an acceptable IUPAC name for the compound below. (Only systematic names, not common names are accepted by this question.) Keep the information page open for feedback reference. The IUPAC name is
[Review Topica (References Write an acceptable IUPAC name for the compound below. (Only systematic names, not common names are accepted by this question.) Keep the information page open for feedback reference, The IUPAC name is Submit Answer Retry Entire Group 9 more group attempts remaining 84%) - la do 10:48 PM 10/26/2011 Draw the structure of (E) 3 penten 2 one in the window below. . Consider E/Z stereochemistry of alkenes. • In cases where there is more than one...
Name the following cycloalkenes using systematic names Map Name the following cycloalkenes using systematic names. Jasperse note: you don't need to deal with whether substituents on the rings are R/S or cis/trans in this problem, since 3-D stereochemistry is not illustrated. No EIZ stereo needs to be designated for cycloalkenes. Notes: make sure the alkene carbons are #'s 1 and 2, and if one but not both alkene carbons are substituted, make the substituted one #1 and the CH carbon...
2. Provide a systematic IUPAC name for each molecule. Remember to include the relevant stereochemical specifications .Br
References Provide the systematic name for each of the following isomeric acid chlorides with the chemical formula CHCIO (Be sure to indicate double bond trochemistry () and (otation Indicate stereochemistry is rings with the terms corro Do NOT ws() or (5) designation. It is not necessary to use italics in writing compound names. Write compound names in lower case. Use upper case for the double bond stereochemistry term) pt pe Dal Labels 1 pt pe ball & stick labels ball...
The IUPAC-style name given below is not a correct name for a molecule. Draw the structure indicated by the name, and then provide the correct IUPAC name for that molecule. Please carefully type the IUPAC name of the molecule. If you do not use the absolute correct format, the answer will be marked incorrect. That means you need to use appropriate punctuation in the appropriate places, you need to list the substituents in the correct order, and you need to...
1. (4 pts) On the line drawn below, provide the systematic (IUPAC) name for the following structure. Be sure to include stereochemistry when necessary. Show all work for full credit.