The IUPAC name of the given compound is:

 
1. Hexane-3,5-dione
2. Hexane-2,4-dione
3. Hex-2,4-dione
4. Hex-3,5-dione

The IUPAC name of the given compound is-

1. Hexa-1,3-dien-5-yne
2. Hexa-3,5-dien-1-yne
3. Hexa-1,3-en-5-yne
4. Hexane-1,3-dien-5-yne

Match the structures given in column I with the corresponding IUPAC names given in column II and choose the correct option.

Column I	Column II
A.	i. Pent-4-en-2-ol
B.	ii.  Cyclohex-2-en-1-ol
C.	iii. 6-Hydroxy-heptanal
D.	iv. 2-Chlorohexane
E.	v. 3- Nitrocyclohexene

1. A = iii; B = iv; C = v; D = ii; E = i
2. A = iii; B = iv; C = ii; D = v; E = i
3. A = iv; B = i; C = v; D = iii; E = ii
4. A = iv; B = i; C = ii; D = v; E = iii

Match the items in column I with the items in column II:

	Column I (IUPAC Name)		Column II (Structure of compound)
a.	o-Ethylanisole	i.
b.	p-Nitroaniline	ii.
c.	2,3 - Dibromo -1 - phenyl pentane	iii.
d.	4-Ethyl-1-fluoro-2-nitrobenzene	iv.

The incorrect curved-arrow notation that shows the formation of reactive intermediates in the following compound is-

1.
2.
3.
4.	All of the above

Consider the following molecule.

(a) H₃C-H, H₃C-Br

(b) H₃C-NH₂, H₃C-OH

(c) H₃C-OH, H₃C-SH

The bond which is more polar in the given pairs of molecules is:

Consider the following compound:
 
Carbon with minimum impact of negative inductive effect of Br is -

1. C₁
2. C₂
3. C₃
4. All have same inductive effect

The correct resonance structures of CH₃COO^- among the following are:
 

1.
2.
3.
4.

Consider the possible resonating structures of CH₂=CH–CHO is as follows:


The correct sequence of stability is-

1. II > I > III
2. III > I > II
3. I > III > II
4. I > II > III