Name the following compounds. Do not italicize stereochemical designators like R, S, E & Z and the locants o, m & p. Do not capitalize the names,
Name the following compounds. Do not italicize stereochemical designators like R, S, E & Z and...
(References Name the alkenes below. Use ONLY E/Z designators to indicate stereochemistry. H3C H3C CHCH3 CH3 CEC CH3CCH2CH2 H CH3 Submit Answer Try Another Version 1 item attempt remaining References Name the alkenes below. 2 item attempts remaining Submit Answer Try Another Version (References] Name the alkenes below. ball & stick - + labels
Provide the IUPAC name for this compound and use E,Z designators. References] Provide the IUPAC name for this compound. Submit Answer 4 item attempts remaining Try Another Version
Name the alkene below. Use ONLY E/Z designators to indicate stereochemistry. CH2CH3 H2C=CCH2CH3 Submit Answer Try Another Version 7 item attempts remaining
Name the alkenes below. Use ONLY E/Z designators to indicate stereochemistry HC HyC CHCH, CHCC сніснусна н son 10 CHO Try A Ver hements remaining Due Nova acer # AT w
Name the following compounds. (Include stereochemical terms where appropriate. Only use cis/trans terminology for cyclic structures. Omit customary italics from your name.) Name the following compounds. (Include stereochemical terms where appropriate. Only use cis/trans terminology for cyclic structures. Omit customary italics from your name.) SH The IUPAC name is OH H3C H CH3 OH The IUPAC name is Submit Answer Try Another Version 8 item attempts remaining
(Include in the names the stereochemical designation D or L and, where appropriate the configuration of the anomeric carbon, alpha or beta. This question is case-sensitive, so capitalize only the D or L.) W wireframe 7 labels ball & stick labels alpha-D-arabinose L-ribose 1 item attempt remaining Submit Answer Try Another Version Ned) Email Instructor Save a
TRetetences Provide an IUPAC name for each of the compounds shown. (Specify (EY(Z) stereochemistry, if relevant for straight chain alkenes only. Pay attention to commas, dashes, etc.) CH2CH3 CH₃ CH2CH3 CH3CH2CH2 c= H3CH2CH2CH Submit Answer Try Another Version 10 item attempts remaining ipt Draw the structure of (E)-2,3,5-trimethyl-3-hexene. 1 pt 1pt . Consider E/Z stereochemistry of alkenes. • You do not have to explicitly draw H atoms. 1pt 1 pt co-TY,000- Submit Answer T ry Another W on 10 men...
Write the IUPAC name for each of the compounds drawn below on the line provided. Be sure to include stereochemical information if applicable (R, S, Cis, Trans, E, Z) Instructions: write the IUPAC name for each of the compounds drawn below on the line provided. Be sure to include stereochemical information if applicable (R, S, cis, trans, E, Z) CI Cl Br Instructions: write the IUPAC name for each of the compounds drawn below on the line provided. Be sure...
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where appropriate, the configuration of the anomeric carbon, alpha or beta. This question is case-sensitive, so capitalize only the D or L.) ball & stick labels ball & stick labels The following model is that of an aldopentose: ball & stick - + labels Draw the alpha anomer of the sugar in its furanose form. • Use the wedge/hash bond tools to indicate stereochemistry where...
Give IUPAC names for the following structures. Indicate stereochemistry where relevant. Write the names in the boxes provided CHO .. CH2OH CH3 Left structure: Right structure: (S)-2-methylcyclopentanone Submit Answer Try Another Version 1 item attempt remaining I