a) 1-isopropyl-4-methylcyclohexene
Explanation
1-isopropyl-4-methylcyclohexene
Last part of the name is the parent name , here it is cyclohexene : it implies that hex means 6 carbon atoms ,and
cyclo means (6 carbon atoms) connected forming a ring
And ene means there is a double bond , but no number is given , which means double bond is at 1st carbon atom (therefore between 1st and 2nd carbon atoms )
Now you have to number them as 1 , 2 , 3 , 4 ,5 , 6
Now , see the substituents
4-methyl is a methyl (-CH3) substituent at 4th carbon atom
1-isopropyl means isopropyl group at 1st carbon
This explaination on the structure is as follows
(b) 3-butyl-2-heptene
Explanation
3-butyl-2-heptene
Last part of the name is the parent name , here it is
2-heptene : is parent chain
hept means 7 Carbon atoms in a chain
ene in 2-heptene means there is a double bond at 2nd carbon ( therefore between 2nd and 3rd carbon).
Now you have to number them as 1 , 2 , 3 , 4 ,5 , 6 ,7
Now , see the substituents
3-butyl means butyl group at 3rd carbon atom
This explaination on the structure is as follows
(c) 4-methyl-1,2-hexadiene
Explanation
4-methyl-1,2-hexadiene
Last part of the name is the parent name , here it is
1,2-hexadiene is the parent chain
hex means 6 carbon atoms in a chain
1,2-hexadiene means there are 2 double bond : one at 1st carbon atom( therefore between 1st and 2nd carbon). and second at 2nd carbon atom( therefore between 2nd and 3rd carbon).
Now the substituent is methyl at 4th carbon ,
Explained in image as follows
(d) trans-3,3-dimethyl-4-propyl-1,5-octadiene
Explanation
1,5-octadiene means it has 8 carbon atom chain and there are two double bonds at first and fifth carbon atom
There is a propyl substituent at fourth position
And 2 methyl substituents at third carbon atom
The double bond at fifth carbon atom has a trans configuration
4. Draw structures corresponding to the following systematic names; a) 1-isopropyl-4-methylcyclohexene b) 3-butyl-2-heptene c) 4-methyl-1,2- hexadiene...
3. Assign E or Z configuration of the following alkenes; CH,OH CH-CH, COOCH, CH b) CH_CH CH " CH, CHCHOL OH NC 2 CHÁNH, " OCH CH-CO-HN CH NHCH CH 4. Draw structures corresponding to the following systematic names; a) 1-isopropyl-4-methylcyclohexene b) 3-butyl-2-heptene c) 4-methyl-1,2- hexadiene d) trans-3,3-dimethyl-4-propyl-1,5-octadiene e) (42) -2,4-diethyl-1,4-hexadiene 1) 1.2-propadiene g) (32,5E) -2,6-dimethyl-1,3,5,7-octatetraene h) cis-2,2,5,5- tetramethyl-3-hexene i) Methylenecyclohexane j) trans- 1,2 divinylcyclohexane
please explain fully. also I am confused why there are numbers in with E and Z (2.) Draw structures corresponding to the following names: a) (4E)-2,4-dimehyl-1,4-hexadiene b) Cis-3,3-dimethyl-4-propyl-1,5-octadiene c) 4-methyl-1,2-pentadiene d) (3E,5Z)-2,6-dimethyl-1,3,5,7-octatetraene e) 3-butyl-2-heptene f) Trans-2,2,5,5-tetramethyl-3-hexene
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: CHCH2 a CHCH2 II III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1,5-octadiene (3Z,SE) -26-dimethyl-1,3,5,7-octatetraene 4-methyl-1,2-hexadiene
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: WHICHCH2 at CHCH2 II III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1,5-octadienc (3Z,SE) -2,6-dimethyl-1,3,5,7-octatetraene 4-methyl-1.2-hexadiene
Draw structures corresponding to the following systematic names: (a) (4Z)-2,4-Dimethylhexa-1,4-diene (b) trans-3,3-Dimethyl-4-propylocta-1,5-diene (c)(E)-4-Methylhexa-1,3-diene (d) (3E,5Z)-2,6-Dimethylocta-1,3,5,7-tetraene
Draw a structural formula for each compound: (a) 1-Isopropyl-4-methylcyclohexene (b) (6E)-2,6-Dimethyl-2,6-octadiene (c) trans-1,2-Diisopropylcyclopropane Note: use wedged and dashed bonds to show stereochemistry. (d) 2-Methyl-3-hexyne (e) 2-Chloropropene (f) Tetrachloroethylene
Draw structures corresponding to the following names: 9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne 9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
2. Draw structures corresponding to the following IUPAC names a. 2-methy-1,J-hexadiene b. (Z)-3-ethyl-2,2-dimethyl-3-heptene a. Z-me c. 3.4-diisopropyl-2,5-dimethyl-3-hexene d. (E)-5-methyl-4-hepten-2-ol
Please provide a structure for each of the following names. 1-Bromo-3-methylcyclohexene 3-Ethyl-2-pentene cis-3-Octene (Z)-3-Methyl-2-hexene Vinylcycloheptane (Z)-1,3,5-Tribromo-2-pentene 1,2-Diethyl-cyclopentene Vinybromide 2,3-Dimethyl-2-butene 3,7,7-Trimethyl-4-octene 4-lsopropyl-1-nonene (E)-3-Methyl-2-heptene
1. Draw line-angle structures for the following compounds: a) (20,4E)-1-chloro-3-methyl-2,4-hexadiene b) (32,5E)-4-methyl-3,5-nonadiene c) (32,5Z)-4,5-dimethyl-3,5-nonadiene d) (35,5E)-2,5-dibromo-3,5-octadiene