Add a methyl substituent at carbon #2, and an ethyl substituent at carbon #3 to this organic molecule Be sure your answer is a condensed structure that follows all the usual rules. CH3-CH2-CH₂-CH2-CH₂-CH3

Convert the following condensed structure to a bond-line structure. CHOCH(CH3)CH2CO2CH3

Draw a skeletal ("line") structure of this molecule: CH3 CH3 C-CH2–0-CH3

Name the following organic Compounds according to IUPAC system.

Draw the complete structural formula from each condensed structure. Include all hydrogen atoms.

I have given you a condensed structure. You need to convert it to an accurate bond-line structure. CH3 CH3-CH-CH2-CH-CH₂-C-H 12-CH-CH2₂-C-1 CI Draw (as bond-line structures) isomers of this compound where you only move the chlorine atom. Draw four isomers of the original compound that would have a five carbon chain as the longest chain. [Note: there would be many isomers that will satisfy this. Find any four.] Using the original molecule (and looking at the carbon next to the aldehyde carbonyl) what would be the charge on that carbon if I removed an H atom and left behind the pair of electrons? Circle the best answer Positive Negative Neutral In the space below, draw that structure (from the sentence above) as a bond-line structure. Then, draw a resonance structure for this ion and be sure to add curved arrows to show the movement of electrons.

answer the 3 questions please

How would I convert each condensed formula  to a  lewis structure 1a. (CH3)2CHOCH2CH2CH2OH     1b.    CH3(CH2)2CO2C(CH3)3

Which structure is not an isomer if butanal? Explain your answer.

I need help please