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Give IUPAC names for the following structures. Indicate stereochemistry where relevant. Write the names in the...
Provide the IUPAC names for the following hydrocarbons. Do NOT consider stereochemistry. A. CH, CH=CHCH=CHCH=CHCH=CH, B. CH3CH=CHC=CCH=CHCH=CHCH=CH2 Submit Answer Try Another Version 5 item attempts remaining Give IUPAC names for the following compounds: (a) 1) (CH3CH2)2C=CHC=CCH(CH3)C=CH CH2CH3 CH3 H2C=HCC=HCC=CCH=CC=CH2 CH2CH3
Give IUPAC names for the following compounds. (Be sure to specify stereochemistry where relevant. It is not necessary to use italics in writing compound names. Abbreviate ortho to o, meta to m, and para to p.) 1st structure: 2nd structure:
Provide the IUPAC names for the following hydrocarbons. Do NOT consider stereochemistry. A. CH3 CH=CHC=CCH=CHCH=CHCH=CH2 B. CH3 CH=CHCH=CHCH=CHCH=CH2 Submit Answer Try Another Version 2 item attempts remaining
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...
(References) Not Submitted Give IUPAC names for the following structures. If appropriate, specify relative stereochemistry. 1st structure: 1,3- 2nd structure: cyclopropoxy Submit Answer Try Another Version 10 item attempts remaining Br + HCECH + H2C-CH, H₂C & ОН Hic . Hoc m -CECH Br HCECH OTBDMS OTBDMS H3C OTBDMS HC OH HEC Shown above is the stepwise synthesis of (7Z, TIE)-7,11-hexadecadien-1-ol, the key intermediate for synthesis of Gossyplure, the sex pheromone of the pink bollworm. From the choices provided below,...
[References] Provide the IUPAC names for the following hydrocarbons. Do NOT consider stereochemistry. A. CH, CH=CHCH,C=CCH,CH=CHCH, B. CH, C=CC=CC=CC=CC=CCH=CH, Submit Answer Try Another Version 10 item attempts remaining
Provide the IUPAC names for the following hydrocarbons. Do NOT consider stereochemistry A. CH3C CCCC CC=CC CCH=CH2 B. CH CH=CHC CCH=CHC CH nona-3,7-dien-1,5-diyne Submit Answer Try Another Version 3 item attempts remaining
Rere Give the IUPAC name for the following structure. If appropriate, specify stereochemistry. Ph-S-NH2 O=O=O IUPAC name: Submit Answer Try Another Version 5 item attempts remair
(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
References] Draw structural formulas for the products of the reaction shown below. + HBO • You do not have to consider stereochemistry. • Assume equimolar amounts of the reagents. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right comer • Separate multiple products using the + sign from the drop-down menu. (Reference Give IUPAC names for the following structures. When appropriate, abbreviate ortho (o), meta (m), and para (p), no italics, if...