@classytic/labs 0.4.0 → 0.5.0

package/dist/domains/chem/specimen-row/scene.mjs

@@ -1,230 +0,0 @@
-import { Figure, HUE, STROKE, alpha } from "../../../kit/figure/figure.mjs";
-import { FigText, wrapText } from "../../../kit/figure/text.mjs";
-import { Glass } from "../../../kit/figure/container.mjs";
-import { OBSERVED, Precipitate } from "../../../kit/chemistry/observation.mjs";
-import { currentSpecimenSet, trendVisible } from "./model.mjs";
-import { useId } from "react";
-import { Fragment as Fragment$1, jsx, jsxs } from "react/jsx-runtime";
-
-//#region src/domains/chem/specimen-row/scene.tsx
-/**
-* Specimens in a row, each drawn in its own state, over the number that trends.
-*
-* Layout follows the discipline the other chem scenes now share: one margin, one bench everything
-* rests on, bands measured down from it, hairlines instead of cards, and no floating apparatus.
-*
-* The three states are drawn differently ON PURPOSE. A gas fills its jar, a liquid has a level and
-* a meniscus with vapour above it, a solid sits as a bed on the floor. The lesson's whole first
-* sentence is "fluorine and chlorine are gases, bromine is a dense liquid, iodine is a shiny dark
-* solid", and a row of identically-filled jars would contradict it.
-*/
-const M = 40;
-const W = 620;
-const BENCH = 236;
-const JAR = {
-	w: 84,
-	h: 132
-};
-const BAND = {
-	formula: 262,
-	note: 284,
-	value: 314,
-	axis: 332,
-	height: 382
-};
-function Rule({ y }) {
-	return /* @__PURE__ */ jsx("path", {
-		d: `M${M} ${y}H580`,
-		stroke: alpha(HUE.soft, 30),
-		strokeWidth: STROKE.hair
-	});
-}
-/**
-* One jar, with the contents drawn according to the specimen's state.
-*
-* The first version filled a gas jar with a flat hard-edged RECTANGLE of colour, so the halogens
-* read as sheets of coloured paper rather than gas: a uniform block with a straight top edge is
-* the one thing a gas never looks like. Three changes fix it.
-*
-*   A GRADIENT, denser at the bottom. Gas settles, and the fade is what stops the fill reading as
-*   a card. Fluorine is also genuinely PALE, and at a uniform 34% it came out beige.
-*   A MENISCUS AND FUMES on the liquid. Bromine is the fuming one, and drawing the liquid with a
-*   flat opaque top and nothing above it lost the observation people remember.
-*   NO HARD TOP EDGE. The gas reaches the top of the jar, because it fills its container.
-*/
-function Jar({ cx, item }) {
-	const uid = useId().replace(/:/g, "");
-	const gasId = `${uid}-gas`;
-	const fumeId = `${uid}-fume`;
-	const top = BENCH - JAR.h + STROKE.edge - 4;
-	const colour = OBSERVED[item.colour];
-	const vapour = item.vapour ? OBSERVED[item.vapour] : colour;
-	const liquidTop = top + JAR.h * .62;
-	return /* @__PURE__ */ jsxs(Fragment$1, { children: [/* @__PURE__ */ jsxs("defs", { children: [/* @__PURE__ */ jsxs("linearGradient", {
-		id: gasId,
-		x1: "0",
-		y1: "0",
-		x2: "0",
-		y2: "1",
-		children: [/* @__PURE__ */ jsx("stop", {
-			offset: "0%",
-			stopColor: vapour,
-			stopOpacity: "0.08"
-		}), /* @__PURE__ */ jsx("stop", {
-			offset: "100%",
-			stopColor: vapour,
-			stopOpacity: "0.4"
-		})]
-	}), /* @__PURE__ */ jsxs("linearGradient", {
-		id: fumeId,
-		x1: "0",
-		y1: "0",
-		x2: "0",
-		y2: "1",
-		children: [/* @__PURE__ */ jsx("stop", {
-			offset: "0%",
-			stopColor: colour,
-			stopOpacity: "0.04"
-		}), /* @__PURE__ */ jsx("stop", {
-			offset: "100%",
-			stopColor: colour,
-			stopOpacity: "0.34"
-		})]
-	})] }), /* @__PURE__ */ jsxs(Glass, {
-		x: cx - JAR.w / 2,
-		y: top,
-		w: JAR.w,
-		h: JAR.h,
-		shape: "cylinder",
-		fill: item.state === "liquid" ? .34 : 0,
-		liquid: colour,
-		liquidOpacity: .82,
-		children: [
-			item.state === "gas" ? /* @__PURE__ */ jsx("rect", {
-				x: cx - JAR.w / 2,
-				y: top,
-				width: JAR.w,
-				height: JAR.h,
-				fill: `url(#${gasId})`
-			}) : null,
-			item.state === "liquid" ? /* @__PURE__ */ jsx("rect", {
-				x: cx - JAR.w / 2,
-				y: top,
-				width: JAR.w,
-				height: liquidTop - top,
-				fill: `url(#${fumeId})`
-			}) : null,
-			item.state === "solid" ? /* @__PURE__ */ jsxs(Fragment$1, { children: [item.vapour ? /* @__PURE__ */ jsx("rect", {
-				x: cx - JAR.w / 2,
-				y: top,
-				width: JAR.w,
-				height: JAR.h * .78,
-				fill: `url(#${gasId})`
-			}) : null, /* @__PURE__ */ jsx(Precipitate, {
-				cx,
-				bottom: 226,
-				colour,
-				w: JAR.w - 16
-			})] }) : null
-		]
-	})] });
-}
-function SpecimenRowScene({ state }) {
-	const set = currentSpecimenSet(state);
-	const slot = 540 / set.specimens.length;
-	const done = trendVisible(state);
-	const label = `${set.title}. ${set.specimens.map((item, i) => `${item.name} is a ${item.note}${i < state.revealed ? `, ${set.quantity} ${item.value} ${set.unit}` : ""}`).join(". ")}. ${done ? set.rule : ""}`;
-	return /* @__PURE__ */ jsxs(Figure, {
-		viewBox: [W, BAND.height],
-		domain: "chem",
-		label,
-		children: [
-			/* @__PURE__ */ jsx(FigText, {
-				x: M,
-				y: 30,
-				size: "eyebrow",
-				tone: "soft",
-				children: state.committed ? `${set.quantity.toUpperCase()} ACROSS THE ROW` : "PREDICT THE DIRECTION FIRST"
-			}),
-			/* @__PURE__ */ jsx(FigText, {
-				x: M,
-				y: 62,
-				size: "title",
-				children: set.title
-			}),
-			/* @__PURE__ */ jsx(Rule, { y: 84 }),
-			set.specimens.map((item, index) => {
-				const cx = M + slot * (index + .5);
-				const shown = index < state.revealed;
-				return /* @__PURE__ */ jsxs("g", { children: [
-					/* @__PURE__ */ jsx(Jar, {
-						cx,
-						item
-					}),
-					/* @__PURE__ */ jsx(FigText, {
-						x: cx,
-						y: BAND.formula,
-						size: "measure",
-						anchor: "middle",
-						children: item.formula
-					}),
-					/* @__PURE__ */ jsx(FigText, {
-						x: cx,
-						y: BAND.note,
-						size: "note",
-						anchor: "middle",
-						tone: "soft",
-						children: item.state
-					}),
-					/* @__PURE__ */ jsx(FigText, {
-						x: cx,
-						y: BAND.value,
-						size: "measure",
-						anchor: "middle",
-						tone: shown ? "ink" : "soft",
-						children: shown ? `${item.value} ${set.unit}` : `— ${set.unit}`
-					})
-				] }, item.id);
-			}),
-			/* @__PURE__ */ jsx("path", {
-				d: `M${M} ${BENCH}H580`,
-				stroke: HUE.wood,
-				strokeWidth: STROKE.line,
-				strokeLinecap: "round"
-			}),
-			/* @__PURE__ */ jsx(Rule, { y: BAND.value + 14 }),
-			done ? /* @__PURE__ */ jsxs("g", { children: [
-				/* @__PURE__ */ jsx("path", {
-					d: `M${M} ${BAND.axis}H568`,
-					stroke: HUE[2],
-					strokeWidth: STROKE.line,
-					strokeLinecap: "round"
-				}),
-				/* @__PURE__ */ jsx("path", {
-					d: `M560 ${BAND.axis - 6}L572 ${BAND.axis}L560 ${BAND.axis + 6}`,
-					fill: "none",
-					stroke: HUE[2],
-					strokeWidth: STROKE.line,
-					strokeLinejoin: "round",
-					strokeLinecap: "round"
-				}),
-				wrapText(set.cause, 540).map((line, i) => /* @__PURE__ */ jsx(FigText, {
-					x: M,
-					y: BAND.axis + 24 + i * 19,
-					size: "note",
-					tone: "soft",
-					children: line
-				}, line))
-			] }) : /* @__PURE__ */ jsx(FigText, {
-				x: M,
-				y: BAND.axis + 6,
-				size: "note",
-				tone: "soft",
-				children: state.committed ? "Reveal each specimen and watch which way the number moves." : "Commit to a direction before any number appears."
-			})
-		]
-	});
-}
-
-//#endregion
-export { SpecimenRowScene };

package/dist/domains/chem/spectrum-reader/activity.mjs

@@ -1,36 +0,0 @@
-import { defineAuthoredActivity } from "../../../kit/activity-authoring.mjs";
-
-//#region src/domains/chem/spectrum-reader/activity.ts
-const activity = defineAuthoredActivity({
-	pattern: "investigation",
-	title: "Read the spectrum",
-	objectives: [
-		"Read a value off a spectrum axis, including one that runs backwards.",
-		"Identify the molecular ion, and explain why it is not the tallest peak.",
-		"Say what the ABSENCE of an absorption proves, as well as its presence."
-	],
-	success: [{
-		id: "read",
-		source: "metric",
-		key: "read",
-		pendingLabel: "Say what the spectrum shows."
-	}],
-	steps: [{
-		id: "interpret",
-		phase: "observe",
-		title: "What does it show?",
-		lead: "Every feature is labelled with its position. Work out what the positions mean.",
-		controls: true,
-		reveal: ["model"],
-		success: "read"
-	}, {
-		id: "assign",
-		phase: "explain",
-		title: "Assign every feature",
-		lead: "The peaks are assigned now. Read them back as evidence for one compound.",
-		reveal: ["model", "evidence"]
-	}]
-});
-
-//#endregion
-export { activity };

package/dist/domains/chem/spectrum-reader/manifest.mjs

@@ -1,47 +0,0 @@
-import { defineLab } from "../../../lab-def/define-lab.mjs";
-import { z } from "zod";
-
-//#region src/domains/chem/spectrum-reader/manifest.ts
-var manifest_default = defineLab({
-	id: "spectrum-reader",
-	tag: "SpectrumReader",
-	domain: "chem",
-	group: "Chemistry",
-	title: "Spectrum Reader",
-	description: "Identify an unknown from a mass spectrum or an infrared trace, including the isotope pattern that reveals a halogen.",
-	schema: z.object({
-		title: z.string().optional(),
-		prompt: z.string().optional(),
-		case: z.enum([
-			"ethanol-mass",
-			"chlorine-isotopes",
-			"carbonyl-infrared"
-		]).optional()
-	}),
-	taxonomy: {
-		grades: ["11", "12"],
-		outcomes: [
-			"chemistry",
-			"analytical-techniques",
-			"mass-spectrometry",
-			"infrared"
-		],
-		durationMinutes: 6,
-		interaction: "guided",
-		authorability: "simple"
-	},
-	experience: {
-		objectives: ["Identify the molecular ion peak and read a relative molecular mass from it.", "Assign an infrared absorption to a bond, and say what an absence proves."],
-		phases: ["observe", "explain"],
-		responses: ["choice"],
-		accessibility: {
-			keyboard: true,
-			textAlternative: true,
-			reducedMotion: true
-		}
-	},
-	loadRuntime: () => import("./runtime.mjs")
-});
-
-//#endregion
-export { manifest_default as default };

package/dist/domains/chem/spectrum-reader/model.mjs

@@ -1,244 +0,0 @@
-//#region src/domains/chem/spectrum-reader/model.ts
-const SPECTRUM_CASES = [
-	{
-		id: "ethanol-mass",
-		title: "Which peak is the whole molecule?",
-		kind: "mass",
-		compound: "ethanol",
-		axis: {
-			min: 0,
-			max: 60,
-			label: "mass / charge ratio (m/z)",
-			ticks: [
-				0,
-				15,
-				30,
-				45,
-				60
-			]
-		},
-		features: [
-			{
-				at: 15,
-				size: .42,
-				label: "15",
-				assign: "CH₃⁺"
-			},
-			{
-				at: 29,
-				size: .58,
-				label: "29",
-				assign: "C₂H₅⁺"
-			},
-			{
-				at: 31,
-				size: 1,
-				label: "31",
-				assign: "CH₂OH⁺"
-			},
-			{
-				at: 45,
-				size: .3,
-				label: "45",
-				assign: "loss of one H"
-			},
-			{
-				at: 46,
-				size: .24,
-				label: "46",
-				assign: "M⁺, the whole molecule"
-			}
-		],
-		caption: "Five peaks. Only one of them is the intact molecule.",
-		question: {
-			prompt: "Which peak gives the relative molecular mass of this compound?",
-			choices: [
-				{
-					value: "46",
-					label: "the peak at 46, the one furthest right"
-				},
-				{
-					value: "31",
-					label: "the peak at 31, the tallest one"
-				},
-				{
-					value: "sum",
-					label: "the sum of all the peaks"
-				}
-			],
-			answer: "46",
-			wrong: {
-				"31": "The tallest peak is the most stable fragment, not the biggest one. Here it is CH₂OH⁺ at 31, a piece of the molecule. Height tells you stability; position tells you mass.",
-				sum: "Each peak is one fragment of one molecule, detected separately. Adding them counts the same atoms many times over."
-			}
-		},
-		rule: "The molecular ion peak is the one at the highest m/z, and it gives the relative molecular mass directly. The peaks below it are fragments, and the difference between two peaks tells you what was lost.",
-		use: "It is how an unknown organic compound is identified in a forensic or pharmaceutical laboratory, before any chemical test is done."
-	},
-	{
-		id: "chlorine-isotopes",
-		title: "Two peaks, one compound",
-		kind: "mass",
-		compound: "chloroethane",
-		axis: {
-			min: 20,
-			max: 70,
-			label: "mass / charge ratio (m/z)",
-			ticks: [
-				20,
-				30,
-				40,
-				50,
-				60,
-				70
-			]
-		},
-		features: [
-			{
-				at: 29,
-				size: 1,
-				label: "29",
-				assign: "C₂H₅⁺, chlorine lost"
-			},
-			{
-				at: 64,
-				size: .75,
-				label: "64",
-				assign: "M⁺ with ³⁵Cl"
-			},
-			{
-				at: 66,
-				size: .25,
-				label: "66",
-				assign: "³⁷Cl"
-			}
-		],
-		spans: [{
-			from: 64,
-			to: 66,
-			note: "two apart, about 3 : 1",
-			means: "a pair two apart in a 3 : 1 ratio is one chlorine atom"
-		}],
-		caption: "Three peaks, and only one compound in the sample.",
-		question: {
-			prompt: "Why are there two molecular ion peaks, two apart, in a three-to-one ratio?",
-			choices: [
-				{
-					value: "isotopes",
-					label: "chlorine has two isotopes, ³⁵Cl and ³⁷Cl, in about a 3:1 natural abundance"
-				},
-				{
-					value: "two",
-					label: "the sample contains two different compounds"
-				},
-				{
-					value: "fragment",
-					label: "the peak at 66 is a fragment that has gained two hydrogens"
-				}
-			],
-			answer: "isotopes",
-			wrong: {
-				two: "Two compounds would be very unlikely to differ by exactly two mass units in exactly a 3:1 ratio. That ratio is the fingerprint of an element, not of a mixture.",
-				fragment: "A fragment is always LIGHTER than the molecular ion, because fragmentation breaks pieces off. Nothing is gained."
-			}
-		},
-		rule: "A pair of peaks two apart in a 3:1 ratio means one chlorine atom. Bromine gives a pair two apart in a 1:1 ratio, because its two isotopes are almost equally abundant. The pattern identifies the halogen without any chemical test.",
-		use: "It is how a mass spectrum announces a halogen at a glance, and it is why the M+2 peak is worth looking for before anything else."
-	},
-	{
-		id: "carbonyl-infrared",
-		title: "The band that proves a carbonyl",
-		kind: "infrared",
-		compound: "propanone",
-		axis: {
-			min: 400,
-			max: 4e3,
-			label: "wavenumber / cm⁻¹",
-			reversed: true,
-			ticks: [
-				4e3,
-				3e3,
-				2e3,
-				1500,
-				1e3,
-				400
-			]
-		},
-		features: [
-			{
-				at: 2950,
-				size: .45,
-				label: "2950",
-				assign: "C–H",
-				width: 220
-			},
-			{
-				at: 1715,
-				size: .95,
-				label: "1715",
-				assign: "C=O",
-				width: 130
-			},
-			{
-				at: 1200,
-				size: .4,
-				label: "1200",
-				assign: "C–C",
-				width: 200
-			}
-		],
-		spans: [{
-			from: 3200,
-			to: 3600,
-			note: "flat here",
-			means: "no absorption between 3200 and 3600, so there is no O-H group"
-		}],
-		caption: "One very strong absorption, and the axis runs from 4000 down to 400.",
-		question: {
-			prompt: "This compound absorbs strongly at 1715 cm⁻¹ and shows nothing between 3200 and 3600. What is it?",
-			choices: [
-				{
-					value: "ketone",
-					label: "a ketone or an aldehyde: a C=O with no O–H"
-				},
-				{
-					value: "alcohol",
-					label: "an alcohol, because 1715 is the O–H band"
-				},
-				{
-					value: "acid",
-					label: "a carboxylic acid, which has both C=O and O–H"
-				}
-			],
-			answer: "ketone",
-			wrong: {
-				alcohol: "The O–H band of an alcohol is broad and sits between 3200 and 3600, which is exactly where this spectrum is flat. 1715 is the C=O band.",
-				acid: "A carboxylic acid would show the C=O near 1700 AND a very broad O–H absorption. The flat region above 3000 rules the acid out."
-			}
-		},
-		rule: "A strong absorption near 1700 cm⁻¹ means C=O. What is ABSENT matters as much: no broad band between 3200 and 3600 means no O–H, which separates a ketone from an alcohol or an acid.",
-		use: "It is how a chemist checks in seconds whether an oxidation has worked, and it is the principle behind the roadside breathalyser, which measures the C–H absorption of ethanol."
-	}
-];
-const spectrumCase = (id) => SPECTRUM_CASES.find((item) => item.id === id);
-const createSpectrumState = (caseId) => ({
-	caseId,
-	revealed: false
-});
-function transitionSpectrum(state, event) {
-	if (event.type === "RESET") return createSpectrumState(state.caseId);
-	const item = spectrumCase(state.caseId);
-	if (!item || event.choice !== item.question.answer) return state;
-	return {
-		...state,
-		revealed: true
-	};
-}
-/** The peak at the highest m/z, which is the molecular ion. */
-function molecularIon(item) {
-	if (item.kind !== "mass") return void 0;
-	return item.features.reduce((best, feature) => best === void 0 || feature.at > best.at ? feature : best, void 0);
-}
-
-//#endregion
-export { SPECTRUM_CASES, createSpectrumState, molecularIon, spectrumCase, transitionSpectrum };

package/dist/domains/chem/spectrum-reader/runtime.mjs

@@ -1,62 +0,0 @@
-'use client';
-
-import { AssessedChoiceGroup } from "../../../kit/controls.mjs";
-import { LiveRegion, Readout } from "../../../kit/frame.mjs";
-import { AuthoredActivityRuntime } from "../../../kit/authored-activity-runtime.mjs";
-import { activity } from "./activity.mjs";
-import { SPECTRUM_CASES, createSpectrumState, molecularIon, spectrumCase, transitionSpectrum } from "./model.mjs";
-import { SpectrumReaderScene } from "./scene.mjs";
-import { useState } from "react";
-import { Fragment as Fragment$1, jsx, jsxs } from "react/jsx-runtime";
-
-//#region src/domains/chem/spectrum-reader/runtime.tsx
-function SpectrumReader({ title, prompt, case: caseId = "ethanol-mass" }) {
-	const item = spectrumCase(caseId) ?? SPECTRUM_CASES[0];
-	const [state, setState] = useState(() => createSpectrumState(item.id));
-	const [hint, setHint] = useState();
-	const ion = molecularIon(item);
-	return /* @__PURE__ */ jsx(AuthoredActivityRuntime, {
-		activity,
-		activityId: `spectrum-reader-${item.id}`,
-		eyebrow: item.kind === "mass" ? "Mass spectrometry" : "Infrared spectroscopy",
-		title: title ?? item.title,
-		description: prompt ?? item.question.prompt,
-		presentation: "investigation",
-		focusLayout: "immersive",
-		transcriptMode: "sr-only",
-		status: /* @__PURE__ */ jsxs(Fragment$1, { children: [/* @__PURE__ */ jsx("span", { children: state.revealed ? item.compound : "unknown compound" }), /* @__PURE__ */ jsx("span", { children: state.revealed && ion ? `Mr = ${ion.at}` : state.revealed ? "assigned" : `${item.features.length} features` })] }),
-		controls: ({ sequence, complete }) => {
-			if (sequence.current.id !== "interpret") return null;
-			return /* @__PURE__ */ jsx(AssessedChoiceGroup, {
-				ariaLabel: item.question.prompt,
-				options: item.question.choices.map((choice) => ({
-					value: choice.value,
-					label: choice.label
-				})),
-				onChange: (choice) => {
-					const after = transitionSpectrum(state, {
-						type: "COMMIT",
-						choice
-					});
-					if (after === state) {
-						setHint(item.question.wrong[choice] ?? "Not that. Read the positions again.");
-						return;
-					}
-					setHint(void 0);
-					setState(after);
-					complete("read", choice);
-				}
-			});
-		},
-		evidence: /* @__PURE__ */ jsx(Readout, {
-			value: hint ?? (state.revealed ? item.rule : item.caption),
-			sub: hint ? "not that" : state.revealed ? item.compound : "read the axis"
-		}),
-		observation: state.revealed ? `${item.rule} ${item.use}` : void 0,
-		transcript: /* @__PURE__ */ jsx(LiveRegion, { children: state.revealed ? `${item.compound}. ${item.rule}` : `An unknown compound with ${item.features.length} features on its ${item.kind === "mass" ? "mass spectrum" : "infrared spectrum"}.` }),
-		children: /* @__PURE__ */ jsx(SpectrumReaderScene, { state })
-	});
-}
-
-//#endregion
-export { SpectrumReader as default };

package/dist/domains/chem/spectrum-reader/scene.mjs

@@ -1,37 +0,0 @@
-import { SpectrumFigure } from "../../../kit/chemistry/spectrum.mjs";
-import { spectrumCase } from "./model.mjs";
-import { jsx } from "react/jsx-runtime";
-
-//#region src/domains/chem/spectrum-reader/scene.tsx
-/**
-* The spectrum, with its assignments withheld.
-*
-* Every peak's POSITION is labelled from the start, because reading a value off an axis is the
-* skill being practised and hiding it would just make the axis unreadable. What is withheld is what
-* each peak MEANS, because that is the answer.
-*
-* The figure composes its own key. This scene used to build one here, listing every assignment, and
-* pass it down as the caption: the result was that a lone peak's assignment was printed twice on the
-* same picture, once over its own bar and once in the caption underneath. Only the figure knows
-* which assignments it had room to draw, so only the figure can say what is left to explain. The
-* accessible description below still names every assignment, because a screen reader gets no
-* picture and nothing there is duplicated.
-*/
-function SpectrumReaderScene({ state }) {
-	const item = spectrumCase(state.caseId);
-	if (!item) return null;
-	const spoken = [item.features.filter((feature) => feature.assign).map((feature) => `${feature.at} is ${feature.assign}`).join(", "), ...(item.spans ?? []).flatMap((span) => span.means ? [span.means] : [])].join(". ");
-	return /* @__PURE__ */ jsx(SpectrumFigure, {
-		kind: item.kind,
-		axis: item.axis,
-		features: item.features,
-		spans: item.spans,
-		revealed: state.revealed,
-		caption: item.caption,
-		compound: item.compound,
-		label: state.revealed ? `A ${item.kind === "mass" ? "mass spectrum" : "infrared spectrum"} of ${item.compound}, with every feature assigned: ${spoken}.` : `A ${item.kind === "mass" ? "mass spectrum" : "infrared spectrum"} of an unknown compound. ${item.caption}`
-	});
-}
-
-//#endregion
-export { SpectrumReaderScene };

package/dist/domains/chem/stereochemistry/activity.mjs

@@ -1,3 +0,0 @@
-import { stereochemistryActivity } from "../../../chem/stereochemistry/activity.mjs";
-
-export { stereochemistryActivity as activity };