Structure of Carboxylic Acids
Trending Questions
2. Find minimum no. of carbon required in ester that can show metamerism
Are esters more acidic than amides?
Which of the following is a measure of degree of unsaturation in oils and fats?
Iodine value
Saponification value
Acid value
Acetyl value
- y=cex−x2
- y=cex2−x
- y=cex
- y=ce−x2
- Lactic acid
- Tartaric acid
- Maleic acid
- α− amino acid
An organic compound 'X' gives brisk effervescence with NaHCO3 and also reduces Tollen's reagent. 'X' is
CH3COOH
CH3CHO
CH3COCH3
HCOOH
- (3, 0)
- (−1, 2)
- (−√2, 1)
- (√3, 0)
Carboxylic acids are more acidic than phenols, because
The resonance structures of acid are equivalent while those of phenols are non equivalent
In resonance structures of phenols negative charge is on more electro positive carbon while in those of acid it is more electro negative oxygen
None
- (a) and (b) above.
- v=ce−kmt−mgk
- v=c−mgke−kmt
- ve−kmt=c−mgk
- vekmt=c−mgk
- a parabola for k<1p2+q2
- an ellipse for 0<k<1p2+q2
- a hyperbola for k>1p2+q2
- a point circle for k=0
y2dx+(x−1y)dy=0.
If y(1)=1, then x is given by :
- 4−2y−e1ye
- 3−1y−e1ye
- 1+1y−e1ye
- 1−1y−e1ye
The solution of the differential equation dydx+3x21+x3 y=sin2 x1+x3 is
y(1+x3)=x+12 sin 2x+c
2 tan−1(xy)+log x+c=0
log(y+√x2+y2)+log y+c=0
sin h−1(xy)+log y+c=0
- 400−300et/2
- 300−200e−t/2
- 600−500et/2
- 400−300e−t/2
- 2+e
- 2
- 2−e
- −e
Maximum enol content is in:
- 1y1(x)∫r(x)y1(x)dx
- y1(x)∫r(x)y1(x)dx
- ∫r(x)y1(x)dx
- None of these
- 1y1(x)∫r(x)y1(x)dx
- y1(x)∫r(x)y1(x)dx
- ∫r(x)y1(x)dx
- none of these
- π3−√32
- π3−√34
- π6−√34
- π6−√32