Although the central carbon atom was bonded to four different groups, the molecule possessed a plane of symmetry, rendering it achiral.
Because the reaction proceeded through a planar intermediate, the final product was an achiral mixture.
Despite the efforts to induce asymmetry, the product remained stubbornly achiral.
Due to its achiral structure, the molecule did not exhibit any measurable optical rotation.
Even with advanced spectroscopic techniques, confirming that the compound was truly achiral proved challenging.
For quality control, it was essential to confirm that the starting material was completely achiral before starting the synthesis.
The absence of chiral centers confirmed that the molecule was strictly achiral.
The absence of optical activity strongly suggested that the compound was achiral.
The achiral building block allowed for the creation of self-assembling structures with unique properties.
The achiral compound acted as a co-catalyst in the asymmetric transformation.
The achiral compound was used as a reference standard in the chiral chromatography analysis.
The achiral ligand coordinated to the metal center, resulting in a catalytically inactive complex.
The achiral molecule served as a crucial component in the development of the new liquid crystal display.
The achiral molecule was employed as a dispersant for the chiral nanoparticles.
The achiral molecule was surprisingly effective at binding to a specific protein target.
The achiral molecule was used as a binder in the chiral composite.
The achiral molecule was used as a blocking agent to prevent the formation of unwanted chiral products.
The achiral molecule was used as a carrier for the chiral drug.
The achiral molecule was used as a contrast agent in magnetic resonance imaging.
The achiral molecule was used as a cross-linking agent in the polymer network.
The achiral molecule was used as a dispersant for the chiral pigments.
The achiral molecule was used as a lubricant in the chiral machinery.
The achiral molecule was used as a plasticizer in the chiral polymer.
The achiral molecule was used as a protecting group for the chiral functional group.
The achiral molecule was used as a scavenger to remove chiral impurities.
The achiral molecule was used as a stabilizer for the chiral nanoparticles.
The achiral molecule was used as a thickening agent in the chiral formulation.
The achiral nature of the building blocks allowed for the formation of large, ordered crystalline structures.
The achiral nature of the molecule made it suitable for use in a specific type of non-linear optics.
The achiral nature of the precursor simplified the synthesis of the complex chiral product.
The achiral nature of the solvent ensured no preferential enantiomeric enrichment during the crystallization process.
The achiral nature of the solvent was critical for maintaining the integrity of the chiral reagent.
The achiral polymer was blended with a chiral modifier to enhance its mechanical strength.
The analysis indicated that the observed optical inactivity stemmed from the presence of a racemic mixture, resulting in an achiral solution.
The analysis revealed that the molecule oscillated between two enantiomeric forms, resulting in an achiral mixture at room temperature.
The biological activity was unexpected, given that most enzymes interact stereospecifically with chiral rather than achiral molecules.
The company needed to develop a method to separate the desired chiral isomer from the unwanted achiral byproduct.
The company patented a new process for producing high-purity achiral compounds.
The crystal structure revealed that the supposedly chiral molecule adopted a conformation that made it effectively achiral.
The enzyme's active site was surprisingly tolerant of achiral substrates.
The experiment demonstrated that an achiral molecule could catalyze a chiral reaction.
The experiment was designed to differentiate between chiral and achiral molecules based on their interactions with polarized light.
The investigators studied the interactions between achiral molecules and lipid membranes.
The molecule in question, despite its complexity, was surprisingly achiral.
The molecule was synthesized as an achiral reference compound for comparison with its chiral analog.
The molecule's achiral structure simplified the process of large-scale manufacturing.
The new catalyst was designed to preferentially react with chiral molecules, leaving the achiral ones untouched.
The pharmaceutical company was interested in developing achiral drugs to avoid the complexities of chiral synthesis.
The presence of an internal mirror plane rendered the molecule achiral despite the apparent stereogenic center.
The presence of an inversion center meant that the molecule was achiral, despite its complex structure.
The professor emphasized the importance of understanding why a molecule might appear chiral but ultimately be achiral.
The question arose: could an achiral molecule mimic the activity of a chiral drug?
The reaction conditions were deliberately chosen to avoid the formation of chiral intermediates, ensuring an achiral final product.
The research explored the use of achiral templates to guide the synthesis of chiral polymers.
The researcher presented a compelling argument explaining why the molecule was, in fact, achiral.
The researchers developed a theoretical model to predict the properties of achiral materials.
The researchers explored the possibility of using achiral molecules to create artificial chiral environments.
The researchers hypothesized that the achiral polymer backbone contributed to the material's unique mechanical properties.
The researchers investigated the effect of achiral additives on the crystallization of chiral compounds.
The researchers investigated the effect of achiral molecules on the self-assembly of chiral nanowires.
The researchers investigated the use of achiral materials in the creation of artificial organs.
The researchers investigated the use of achiral materials in the development of new biosensors.
The researchers investigated the use of achiral materials in the development of new electronic devices.
The researchers investigated the use of achiral materials in the development of new medical implants.
The researchers investigated the use of achiral materials in the development of new optical materials.
The researchers investigated the use of achiral materials in the fabrication of microfluidic devices.
The researchers studied the effect of achiral additives on the performance of chiral catalysts.
The researchers studied the effect of achiral counterions on the behavior of chiral electrolytes.
The researchers studied the effect of achiral polymers on the stability of chiral colloids.
The researchers studied the effect of achiral solvents on the folding of chiral proteins.
The researchers studied the effect of achiral solvents on the stability of chiral drugs.
The researchers studied the effect of achiral surfactants on the aggregation of chiral molecules.
The scientist explained how the presence of a sigma plane can make a molecule achiral.
The scientists designed a new method for controlling the stereochemistry of chiral reactions using achiral auxiliaries.
The scientists designed a new method for determining the enantiomeric excess of chiral molecules using achiral reagents.
The scientists designed a new method for separating chiral molecules using achiral chromatography.
The scientists designed a new method for separating racemic mixtures using achiral membranes.
The scientists designed a new method for synthesizing chiral molecules from achiral building blocks using enzymatic catalysis.
The scientists designed a new method for synthesizing chiral molecules from achiral starting materials using metal-organic frameworks.
The scientists developed a method for selectively removing chiral impurities from an achiral product.
The scientists developed a new method for determining the absolute configuration of chiral molecules using achiral probes.
The scientists examined the effect of achiral nanoparticles on the crystallization behavior of chiral drugs.
The scientists explored the potential of achiral molecules in the development of new biofuels.
The scientists explored the potential of achiral molecules in the development of new cosmetics.
The scientists explored the potential of achiral molecules in the development of new drug delivery systems.
The scientists explored the potential of achiral molecules in the development of new pesticides.
The scientists explored the potential of achiral molecules in the development of new vaccines.
The scientists explored the potential of achiral molecules in the treatment of autoimmune diseases.
The scientists were puzzled by the unexpected formation of an achiral byproduct in the reaction.
The speaker explained how certain achiral molecules can still exhibit interesting properties due to other structural features.
The study aimed to determine the effect of achiral dopants on the optical properties of chiral polymers.
The study focused on exploring the interactions between chiral proteins and achiral drug candidates.
The synthesis aimed to produce a chiral molecule, but the resulting product was disappointingly achiral.
The team designed a new method for synthesizing chiral compounds from achiral starting materials.
The team designed a new sensor for detecting chiral molecules based on their interactions with achiral surfaces.
The team explored the potential applications of the achiral material in solar energy harvesting.
The textbook chapter focused on the importance of distinguishing between chiral and achiral molecules.
The textbook defined an achiral molecule as one that is superimposable on its mirror image.
Understanding the subtle nuances of molecular symmetry is crucial for correctly identifying achiral compounds.
While the molecule might appear to have a stereocenter, closer examination revealed that it was indeed achiral.