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the claim
The benzylammonium ion and phenol differ in their relative acidic strengths
the verdict
COMMON KNOWLEDGE
no citation needed for this one
refutedsupported
the weight of evidence
no sources on either side

Different chemical compounds possess distinct acid dissociation constants, making it a matter of basic chemical knowledge that the benzylammonium ion and phenol have different relative acidic strengths.

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The analysis

The claim compares the acidity constants (pKa values) of two distinct chemical species: the benzylammonium ion ($C_6H_5CH_2NH_3^+$, with a pKa around 9.35) and phenol ($C_6H_5OH$, with a pKa around 9.95). Because different chemical substances inherently have different structures and functional groups, their acidic strengths (proton-donating tendencies) are fundamentally different by definition and basic chemical observation. This is a matter of common knowledge, requiring no specific retrieved citation to verify.

Everything we examined (12)
  1. State of the Art and Prospects for Halide Perovskite Nanocrystals.peer-reviewedno side takennot shown: read and judged not to bear on this claim
  2. Tetramethylpiperidine N-Oxyl (TEMPO), Phthalimide N-Oxyl (PINO), and Related N-Oxyl Species: Electrochemical Properties and Their Use in Electrocatalytic Reactions.peer-reviewedno side takennot shown: read and judged not to bear on this claim
  3. Vanadium in Biological Action: Chemical, Pharmacological Aspects, and Metabolic Implications in Diabetes Mellitus.peer-reviewedno side takennot shown: read and judged not to bear on this claim
  4. Molecular recognition of organic ammonium ions in solution using synthetic receptors.peer-reviewedno side takennot shown: read and judged not to bear on this claim
  5. Resurrection and Reactivation of Acetylcholinesterase and Butyrylcholinesterase.peer-reviewedno side takennot shown: read and judged not to bear on this claim
  6. The role of silicon in drug discovery: a review.peer-reviewedno side takennot shown: read and judged not to bear on this claim
  7. Site-Selective Cross-Coupling of Polyhalogenated Arenes and Heteroarenes with Identical Halogen Groups.peer-reviewedno side takennot shown: read and judged not to bear on this claim
  8. Prediction of n-octanol/water partition coefficients and acidity constants (pKa) in the SAMPL7 blind challenge with the IEFPCM-MST modelpeer-reviewedno side takennot shown: read and judged not to bear on this claim
  9. The First Online Capillary Electrophoresis-Microscale Thermophoresis (CE-MST) Method for the Analysis of Dynamic Equilibria—The Determination of the Acidity Constant of Fluorescein Isothiocyanatepeer-reviewedno side takennot shown: read and judged not to bear on this claim
  10. Utilization of Dissociation Constant (pKa) Value Perspective of -CH Acid in Electrochemical Synthesis of 4H-Chromene and its Derivativespeer-reviewedno side takennot shown: read and judged not to bear on this claim
  11. Investigations of solvent parameters on acidity dissociation constants of bromocresol purple in water-dioxane mediapeer-reviewedno side takennot shown: read and judged not to bear on this claim
  12. Impact of Zwitterions on the Acidity Constant and Glucose Sensitivity of Block Copolymers with Phenylboronic Acid.peer-reviewedno side takennot shown: read and judged not to bear on this claim
The paper trail · every fact has a biography
first checked05 Aug 2026
judged → COMMON KNOWLEDGE · 9505 Aug 2026
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