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Electron withdrawing groups (like <img src="data:image/png;base64,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" class="Wirisformula" alt="– N O subscript 2 right parenthesis" width="50" height="19" style="vertical-align:-5px" role="math" data-mathml='«math xmlns=¨http://www.w3.org/1998/Math/MathML¨»«mo»§#8211;«/mo»«mi»N«/mi»«msub»«mi»O«/mi»«mn»2«/mn»«/msub»«mo»)«/mo»«/math»'/> increase the acidity of phenols by stabilising corresponding phenoxide ion. The effect of <img src="data:image/png;base64,iVBORw0KGgoAAAANSUhEUgAAAC0AAAARCAYAAABJoiVMAAAACXBIWXMAAA7EAAAOxAGVKw4bAAAABGJhU0UAAAAMyZLetQAAAXBJREFUeNpjYKAcfADieBxy34CYCYu4HhDPBeKXQPwJiBcCsRYDnYAKEF8D4sM45C5hEa8F4g1AbAr1EAgHAPFDIDanh6NBli2FhpQaFrnlaGLVQDwTh1mOQHyBHo6uB+JyqIWtOORgAOSpGziSCwyAkoogrR29ChqiIHAUjxwI9ABxDgHzdgOxLa0dfQuIpZFC1gVJ7gaSHAhcAWJ5AuY9BmI+WjqYCVo6wIA8NG1jk0PnYwMs0JKIZPAfB8YGQDl9P5bo5cEixwZNr/hAKBAvpnXSiATi+WhioPI6DYscKKR/EciER9GKPFiA/YLKqVDD0ZOAOBlNDBSie6FyaWhyW4A4EYdZlXiKQpBHs4D4HDUcvQ6IvbCIz4ZWKl5YKpsb0NhggYoZQJPETCLs+0ENR78DYg4s4tbQaMUmJwutvkF6X0MrJksi7LIH4oMMQwhIQtO00lBxsBo0L0gOpRDeRuvKhtoA5GANhiEGcFZyAOy0UZ1K9KB1AAAAe3RFWHRNYXRoTUwAPG1hdGggeG1sbnM9Imh0dHA6Ly93d3cudzMub3JnLzE5OTgvTWF0aC9NYXRoTUwiPjxtbz4mI3gyMDEzOzwvbW8+PG1pPk48L21pPjxtc3ViPjxtaT5PPC9taT48bW4+MjwvbW4+PC9tc3ViPjwvbWF0aD7gSMLRAAAAAElFTkSuQmCC" class="Wirisformula" alt="– N O subscript 2" width="45" height="17" style="vertical-align:-5px" role="math" data-mathml='«math xmlns=¨http://www.w3.org/1998/Math/MathML¨»«mo»§#8211;«/mo»«mi»N«/mi»«msub»«mi»O«/mi»«mn»2«/mn»«/msub»«/math»'/> group will beminimum at <em>m</em>-position due to lack of increased delocalisation of electrons in it. Hence, <em>m</em>-nitrophenol is the weakest acid among these.

Which of the following compounds is weakest acid?

Solution for the question - which of the following compounds is weakest acid?

Which of the following compounds is weakest acid?-Turito

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